Tatiana Foroud | Academic Influence

Tatiana Foroud's Degrees

PhD Medical & Molecular Genetics Purdue University

Why Is Tatiana Foroud Influential?

According to Wikipedia, Tatiana Foroud is a genetic researcher and currently the Joe C. Christian Professor Medical and Molecular Genetics, Distinguished Professor and Chancellor's Professor at the Indiana University School of Medicine.

(See a Problem?)

Tatiana Foroud's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2013) (3484)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura (2001) (1663)
Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease (2011) (1656)
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease (2014) (1591)
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease (2014) (1230)
Common genetic determinants of vitamin D insufficiency: a genome-wide association study (2010) (1177)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (1073)
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
Genome-wide search for genes affecting the risk for alcohol dependence. (1998) (738)
Common genetic variants influence human subcortical brain structures (2015) (731)
Early role of vascular dysregulation on late-onset Alzheimer's disease based on multifactorial data-driven analysis (2016) (716)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (2017) (693)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
Variations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations. (2004) (659)
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 (1988) (648)
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) (646)
Identification of common variants associated with human hippocampal and intracranial volumes (2012) (617)
Variants in nicotinic receptors and risk for nicotine dependence. (2008) (612)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. (2003) (592)
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database (2012) (546)
A genome-wide association study of alcohol dependence (2010) (544)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. (1998) (497)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease (2005) (459)
Genomewide association study for susceptibility genes contributing to familial Parkinson disease (2009) (446)
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. (2010) (426)
Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders (2018) (372)
Genetics of Parkinson disease (2004) (363)
Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans (2010) (360)
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. (2013) (357)
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort (2010) (351)
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. (2013) (345)
Diagnostic value of plasma phosphorylated tau181 in Alzheimer’s disease and frontotemporal lobar degeneration (2020) (322)
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis (2012) (308)
Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus (2002) (294)
Genome-wide association study of alcohol dependence implicates a region on chromosome 11. (2010) (292)
Translation initiator EIF4G1 mutations in familial Parkinson disease. (2011) (290)
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32 (1997) (279)
Common variants at MS 4 A 4 / MS 4 A 6 E , CD 2 AP , CD 33 and EPHA 1 are associated with late-onset Alzheimer ’ s disease (2011) (274)
Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2 (2012) (274)
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (270)
Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families (2012) (270)
Progression of symptoms in the early and middle stages of Huntington disease. (2001) (269)
Voxelwise genome-wide association study (vGWAS) (2010) (269)
Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis. (2006) (262)
Genetic predisposition to external apical root resorption. (2003) (261)
Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping. (2000) (255)
Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension. (1995) (254)
A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly (2010) (248)
New insights into the genetic etiology of Alzheimer’s disease and related dementias (2022) (246)
A NOVEL ALZHEIMER DISEASE LOCUS LOCATED NEAR THE GENE ENCODING TAU PROTEIN (2015) (246)
Mutations in COQ2 in familial and sporadic multiple-system atrophy. (2013) (246)
Candidate genes for alcohol dependence: a review of genetic evidence from human studies. (2003) (245)
Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
Novel genetic loci associated with hippocampal volume (2017) (238)
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. (2005) (235)
The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort (2018) (234)
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease (2018) (233)
Differences in duration of Huntington’s disease based on age at onset (1999) (231)
The Role of GABRA2 in Risk for Conduct Disorder and Alcohol and Drug Dependence across Developmental Stages (2006) (230)
An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians. (1998) (229)
Genome-Wide Association of Familial Late-Onset Alzheimer's Disease Replicates BIN1 and CLU and Nominates CUGBP2 in Interaction with APOE (2011) (226)
Lessons Learned from Whole Exome Sequencing in Multiplex Families Affected by a Complex Genetic Disorder, Intracranial Aneurysm (2015) (221)
Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans (2015) (219)
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease (2003) (218)
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset (2009) (217)
Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12. (1997) (215)
Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. (2003) (212)
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. (2000) (212)
A genome screen of maximum number of drinks as an alcoholism phenotype. (2000) (210)
REVIEW: The genetics of alcoholism: identifying specific genes through family studies (2006) (210)
A genome-wide search for genes that relate to a low level of response to alcohol. (2001) (209)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Guidelines for the standardization of preanalytic variables for blood-based biomarker studies in Alzheimer's disease research (2015) (205)
Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder. (2001) (204)
Basal forebrain degeneration precedes and predicts the cortical spread of Alzheimer's pathology (2016) (201)
Four distinct trajectories of tau deposition identified in Alzheimer’s disease (2021) (200)
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene (1992) (199)
Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. (1999) (198)
Identification of pathways for bipolar disorder: a meta-analysis. (2014) (197)
ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry (2011) (197)
A quantitative trait locus for alcohol consumption in selectively bred rat lines. (1998) (197)
Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians. (1998) (196)
Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study (2019) (194)
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. (2002) (193)
Novel genetic loci underlying human intracranial volume identified through genome-wide association (2016) (192)
Association of GABRA2 with Drug Dependence in the Collaborative Study of the Genetics of Alcoholism Sample (2006) (188)
APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study (2013) (184)
Copy-number disorders are a common cause of congenital kidney malformations. (2012) (182)
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats (2013) (176)
Genome-wide association study of CSF biomarkers Aβ1-42, t-tau, and p-tau181p in the ADNI cohort (2010) (175)
Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. (1997) (174)
Quantitative trait loci analysis of human event-related brain potentials: P3 voltage. (1998) (174)
Convergent genetic and expression data implicate immunity in Alzheimer's disease (2014) (172)
Enrichment of Cis-Regulatory Gene Expression SNPs and Methylation Quantitative Trait Loci Among Bipolar Disorder Susceptibility Variants (2012) (165)
Genetics of osteoporosis. (2002) (162)
Meta‐Analysis of Genome‐Wide Scans Provides Evidence for Sex‐ and Site‐Specific Regulation of Bone Mass (2006) (161)
Ferritin levels in the cerebrospinal fluid predict Alzheimer's disease outcomes and are regulated by APOE (2015) (161)
Singleton deletions throughout the genome increase risk of bipolar disorder (2009) (159)
Greater Rupture Risk for Familial as Compared to Sporadic Unruptured Intracranial Aneurysms (2009) (159)
Significant linkage of Parkinson disease to chromosome 2q36-37. (2003) (158)
Genetic Predisposition to External Apical Root Resorption in Orthodontic Patients: Linkage of Chromosome-18 Marker (2003) (157)
Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease (2010) (156)
Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study (2013) (155)
Association of the κ-opioid system with alcohol dependence (2006) (154)
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. (2016) (153)
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers (2013) (153)
Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene Group. (1997) (150)
Transethnic genome-wide scan identifies novel Alzheimer's disease loci (2017) (149)
Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (148)
Anxiety proneness linked to epistatic loci in genome scan of human personality traits. (1998) (148)
Pooled association genome scanning for alcohol dependence using 104,268 SNPs: Validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the genetics of alcoholism (2006) (148)
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. (2003) (147)
Linkage of a QTL Contributing to Normal Variation in Bone Mineral Density to Chromosome 11q12–13 (1998) (146)
Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition. (2004) (144)
Identification of TMEM230 mutations in familial Parkinson’s disease (2016) (143)
Association of GABRG3 with alcohol dependence. (2004) (142)
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. (2014) (140)
Subtle changes among presymptomatic carriers of the Huntington's disease gene (2000) (138)
APOE effect on Alzheimer's disease biomarkers in older adults with significant memory concern (2015) (138)
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease (2008) (137)
Racial Disparities in Adverse Pregnancy Outcomes and Psychosocial Stress. (2018) (137)
The role of apolipoprotein E (APOE) genotype in early mild cognitive impairment (E-MCI) (2013) (137)
Endophenotypes Successfully Lead to Gene Identification: Results from the Collaborative Study on the Genetics of Alcoholism (2006) (136)
Predicting Alzheimer’s disease progression using multi-modal deep learning approach (2019) (136)
Amplitude of visual P3 event-related potential as a phenotypic marker for a predisposition to alcoholism: preliminary results from the COGA Project. Collaborative Study on the Genetics of Alcoholism. (1998) (135)
Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence. (2006) (132)
Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment (2014) (131)
Genetics and alcoholism (2013) (131)
Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure (2001) (126)
α-Synuclein maps to a quantitative trait locus for alcohol preference and is differentially expressed in alcohol-preferring and -nonpreferring rats (2003) (126)
Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci. (2008) (126)
Voxelwise gene-wide association study (vGeneWAS): Multivariate gene-based association testing in 731 elderly subjects (2011) (125)
Predicting Sensation Seeking From Dopamine Genes (2010) (125)
Marital status, alcohol dependence, and GABRA2: evidence for gene-environment correlation and interaction. (2006) (124)
Cognitive scores in carriers of huntington's disease gene compared to noncarriers (1995) (124)
Predictive Accuracy of Serial Transvaginal Cervical Lengths and Quantitative Vaginal Fetal Fibronectin Levels for Spontaneous Preterm Birth Among Nulliparous Women (2017) (124)
A genomic scan for habitual smoking in families of alcoholics: Common and specific genetic factors in substance dependence (2004) (124)
Association of the kappa-opioid system with alcohol dependence. (2006) (120)
A description of the methods of the Nulliparous Pregnancy Outcomes Study: monitoring mothers-to-be (nuMoM2b). (2015) (118)
Saccades in presymptomatic and early stages of Huntington disease (2006) (118)
Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X. (1997) (117)
Genomewide association study for onset age in Parkinson disease (2009) (116)
TREM2 is associated with increased risk for Alzheimer’s disease in African Americans (2015) (116)
A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors. (2005) (114)
Longitudinal Change of Clinical and Biological Measures in Early Parkinson's Disease: Parkinson's Progression Markers Initiative Cohort (2018) (113)
Association of GABAA receptors and alcohol dependence and the effects of genetic imprinting (2003) (113)
A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism. (1998) (111)
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry (2017) (110)
Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk (2012) (109)
GWAS of longitudinal amyloid accumulation on 18F-florbetapir PET in Alzheimer's disease implicates microglial activation gene IL1RAP. (2015) (108)
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. (1999) (108)
Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking. (2000) (107)
Screening for brain aneurysm in the Familial Intracranial Aneurysm study: frequency and predictors of lesion detection. (2008) (106)
C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease. (2013) (105)
Alcohol dehydrogenase-2*2 allele is associated with decreased prevalence of fetal alcohol syndrome in the mixed-ancestry population of the Western Cape Province, South Africa. (2001) (105)
Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases (2012) (104)
A large-scale genome-wide association study meta-analysis of cannabis use disorder (2020) (104)
A large-scale genome-wide association study meta-analysis of cannabis use disorder (2020) (104)
Facial Dysmorphism Across the Fetal Alcohol Spectrum (2013) (103)
A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence. (1998) (102)
Genomic Survey of Bipolar Illness in the NIMH Genetics Initiative Pedigrees: A Preliminary Report (1997) (101)
The Alzheimer's Disease Sequencing Project: Study design and sample selection (2017) (101)
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory (2012) (101)
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture (2021) (99)
Genomic screen for QTLs underlying alcohol consumption in the P and NP rat lines (1998) (99)
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. (2006) (98)
Association between GABRA1 and drinking behaviors in the collaborative study on the genetics of alcoholism sample. (2006) (97)
Variants associated with Gaucher disease in multiple system atrophy (2015) (97)
Finding useful biomarkers for Parkinson’s disease (2018) (96)
Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia (2006) (96)
Functional brain architecture is associated with the rate of tau accumulation in Alzheimer’s disease (2020) (96)
Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women (2004) (96)
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts (2016) (94)
Association of the angiotensinogen gene to serum angiotensinogen in blacks and whites. (1997) (93)
Prenatal alcohol exposure alters the patterns of facial asymmetry. (2010) (92)
Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans (2014) (92)
Collaborative initiative on fetal alcohol spectrum disorders: methodology of clinical projects. (2010) (92)
Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199 (2015) (91)
Chloride Channel 7 (ClCN7) Gene Mutations and Autosomal Dominant Osteopetrosis, Type II (2003) (91)
Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence. (2008) (91)
Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD (2013) (91)
The opioid system in alcohol and drug dependence: Family‐based association study (2007) (90)
Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees (2003) (90)
Suggestive linkage on chromosome 1 for a quantitative alcohol-related phenotype. (2002) (90)
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks (2013) (89)
Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q. (1997) (89)
Association of NFKB1, which encodes a subunit of the transcription factor NF-kappaB, with alcohol dependence. (2007) (88)
Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals (2012) (88)
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis. (2020) (86)
Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations. (2007) (85)
Mapping and characterization of structural variation in 17,795 human genomes (2020) (84)
Meta‐analysis of genome‐wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women (2013) (84)
Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes (2011) (81)
Stress-response pathways are altered in the hippocampus of chronic alcoholics. (2013) (81)
Functional relevance of human adh polymorphism. (2001) (81)
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. (1997) (81)
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. (2012) (81)
The North American Multiple System Atrophy Study Group (2005) (80)
A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53 (2013) (80)
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations (2009) (80)
Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family Study. (2011) (79)
Longitudinal personality changes among presymptomatic Huntington disease gene carriers. (2002) (79)
Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence (2009) (79)
Association of Alcohol Craving With α‐Synuclein (SNCA) (2007) (79)
Genetic Effects for Femoral Biomechanics, Structure, and Density in C57BL/6J and C3H/HeJ Inbred Mouse Strains (2003) (79)
Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample. (2008) (78)
Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene. (2000) (78)
Copy Number Variation in Familial Parkinson Disease (2011) (78)
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2019) (77)
Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women. (2010) (77)
Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees. (2000) (77)
Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington’s disease (2003) (76)
Variability in Skeletal Mass, Structure, and Biomechanical Properties Among Inbred Strains of Rats (2001) (76)
A mutation in myotilin causes spheroid body myopathy (2005) (75)
Specific psychiatric manifestations among preclinical Huntington disease mutation carriers. (2007) (75)
Linkage of an alcoholism-related severity phenotype to chromosome 16. (1998) (75)
Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women (2005) (75)
A regulatory variation in OPRK1, the gene encoding the κ-opioid receptor, is associated with alcohol dependence (2008) (75)
Non-coding variability at the APOE locus contributes to the Alzheimer’s risk (2019) (74)
Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event‐related oscillations and alcohol dependence (2009) (74)
Validation of Serum Neurofilament Light Chain as a Biomarker of Parkinson’s Disease Progression (2020) (73)
Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men. (2005) (73)
Gene Expression Profiles in Parkinson Disease Prefrontal Cortex Implicate FOXO1 and Genes under Its Transcriptional Regulation (2012) (72)
APOE ε4 and the risk for Alzheimer disease and cognitive decline in African Americans and Yoruba (2014) (72)
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study (2020) (71)
Functional microRNAs in Alzheimer’s disease and cancer: differential regulation of common mechanisms and pathways (2013) (71)
Genome‐wide association study of theta band event‐related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence (2011) (71)
Association of Blood Biomarkers With Acute Sport-Related Concussion in Collegiate Athletes (2020) (70)
Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence (2017) (70)
Peroxisome proliferator-activated receptors α and γ are linked with alcohol consumption in mice and withdrawal and dependence in humans. (2015) (70)
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. (1999) (70)
Genetic influences on craving for alcohol. (2013) (70)
AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia (2015) (70)
Robust Identification of Alzheimer’s Disease subtypes based on cortical atrophy patterns (2017) (69)
Motor changes in presymptomatic Huntington disease gene carriers. (1996) (69)
Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence. (2010) (69)
Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees (2004) (68)
Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: a preliminary report. (1996) (68)
A Cholinergic Receptor Gene (CHRM2) Affects Event-related Oscillations (2006) (67)
The Familial Intracranial Aneurysm (FIA) study protocol (2005) (67)
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans (2017) (67)
Genome-wide pathway analysis of memory impairment in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort implicates gene candidates, canonical pathways, and networks (2012) (67)
A polymorphism in GABRA2 is associated with the medial frontal response to alcohol cues in an fMRI study. (2010) (66)
Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. (2012) (66)
Polygenic Risk for Externalizing Disorders (2015) (66)
Localization of an ataxia-telangiectasia gene to an ∼500-kb interval on chromosome 11q23.1 : linkage analysis of 176 families by an international consortium (1991) (65)
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study (2016) (65)
Whole-Exome Sequencing in Familial Parkinson Disease. (2016) (62)
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction (2021) (62)
Possible localization of a major gene for cleft lip and palate to 4q (1994) (61)
Ten‐year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease (2008) (61)
Multiple step pattern as a biomarker in Parkinson disease. (2009) (61)
Influence of ADH1B polymorphism on alcohol use and its subjective effects in a Jewish population. (2002) (60)
Root resorption associated with orthodontic force in inbred mice: genetic contributions. (2006) (60)
Targeted neurogenesis pathway-based gene analysis identifies ADORA2A associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease (2017) (60)
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans (2012) (59)
Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study (2011) (59)
Parkinson Disease Overview (2014) (58)
The search for genetic risk factors associated with suicidal behavior. (2004) (58)
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium (2019) (58)
Genome-Wide Association Study for Anthracycline-Induced Congestive Heart Failure (2016) (58)
Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families (2002) (58)
Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism. (2001) (57)
Recent drinking history: association with family history of alcoholism and the acute response to alcohol during a 60 mg% clamp. (2002) (57)
Identification of Quantitative Trait Loci Influencing Alcohol Consumption in the High Alcohol Drinking and Low Alcohol Drinking Rat Lines (2000) (57)
Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder (2008) (57)
Protective variant for hippocampal atrophy identified by whole exome sequencing (2015) (56)
Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology (2020) (56)
Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium (2020) (56)
Comparison of Parent, Peer, Psychiatric, and Cannabis Use Influences Across Stages of Offspring Alcohol Involvement: Evidence from the COGA Prospective Study (2017) (56)
Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism (2018) (55)
Shared genetic contribution to ischemic stroke and Alzheimer's disease (2016) (55)
Peak bone mineral density at the hip is linked to chromosomes 14q and 15q (2004) (55)
Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women. (2004) (55)
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation (2014) (54)
Genetic associations with taxane-induced neuropathy by a genome-wide association study (GWAS) in E5103. (2011) (54)
Association of alcohol craving with alpha-synuclein (SNCA). (2007) (54)
Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials. (2016) (54)
Influence of Genetic Variation on Plasma Protein Levels in Older Adults Using a Multi-Analyte Panel (2013) (54)
Genome-Wide Association Study of Intracranial Aneurysm Identifies a New Association on Chromosome 7 (2014) (53)
Variation in GIGYF2 is not associated with Parkinson disease (2009) (53)
Genome Screen to Detect Linkage to Intracranial Aneurysm Susceptibility Genes: The Familial Intracranial Aneurysm (FIA) Study (2008) (53)
Neurology Individualized Medicine: When to Use Next-Generation Sequencing Panels. (2017) (53)
The BIN1 rs744373 SNP is associated with increased tau-PET levels and impaired memory (2019) (52)
Inflammatory profile in LRRK2-associated prodromal and clinical PD (2016) (52)
Amyloid pathway-based candidate gene analysis of [11C]PiB-PET in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort (2011) (52)
Prenatal alcohol exposure: advancing knowledge through international collaborations. (2003) (52)
Polygenic risk scores in familial Alzheimer disease (2017) (52)
Family‐based genome‐wide association study of frontal theta oscillations identifies potassium channel gene KCNJ6 (2012) (52)
Mutations in DJ-1 are rare in familial Parkinson disease (2006) (51)
Lack of association of alcohol dependence and habitual smoking with catechol-O-methyltransferase. (2007) (50)
In vivo distribution of α-synuclein in multiple tissues and biofluids in Parkinson disease (2020) (50)
Genetics of alcoholism: a review of recent studies in human and animal models. (1999) (50)
Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women. (2005) (50)
Polygenic Risk for Externalizing Disorders: Gene-by-Development and Gene-by-Environment Effects in Adolescents and Young Adults (2015) (50)
Association of substance dependence phenotypes in the COGA sample (2015) (49)
Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region. (1990) (49)
Is There a Genetic Relationship Between Alcoholism and Depression? (2002) (49)
The Relationship Between Smoking and Replicated Sequence Variants on Chromosomes 8 and 9 With Familial Intracranial Aneurysm (2010) (49)
Facial Dysmorphism Across the Fetal Alcohol (2016) (49)
Heterogeneity in hereditary pancreatitis. (1998) (48)
Age-specific incidence rates for dementia and Alzheimer disease in NIA-LOAD/NCRAD and EFIGA families: National Institute on Aging Genetics Initiative for Late-Onset Alzheimer Disease/National Cell Repository for Alzheimer Disease (NIA-LOAD/NCRAD) and Estudio Familiar de Influencia Genetica en Alzhei (2014) (48)
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease (2015) (48)
Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X (2003) (48)
Genetic Strategies to Detect Genes Involved in Alcoholism and Alcohol-Related Traits (2002) (47)
The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease. (2016) (46)
The tachykinin receptor 3 is associated with alcohol and cocaine dependence. (2008) (46)
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
GABRR1 and GABRR2, encoding the GABA‐A receptor subunits ρ1 and ρ2, are associated with alcohol dependence (2010) (45)
Age-at-Onset in Late Onset Alzheimer Disease is Modified by Multiple Genetic Loci (2014) (44)
Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis. (2008) (44)
Progression in prediagnostic Huntington disease (2009) (44)
Genome-wide scan for a healthy aging phenotype provides support for a locus near D4S1564 promoting healthy aging. (2004) (44)
The Systemic Synuclein Sampling Study: toward a biomarker for Parkinson's disease. (2017) (44)
A Systematic Single Nucleotide Polymorphism Screen to Fine-Map Alcohol Dependence Genes on Chromosome 7 Identifies Association With a Novel Susceptibility Gene ACN9 (2008) (43)
The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23. (1991) (43)
HUMAN GENETIC STUDY: Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence (2008) (43)
Genome scan of the fifty‐six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21 (2003) (43)
Genetics of bipolar affective disorder (2000) (43)
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8 (2007) (42)
Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study. (2010) (42)
NIPT and Informed Consent: an Assessment of Patient Understanding of a Negative NIPT Result (2016) (42)
Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts (2010) (42)
Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus. (2000) (42)
Linkage of Structure at the Proximal Femur to Chromosomes 3, 7, 8, and 19 (2003) (42)
Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior (2015) (42)
Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100 (2014) (41)
Chromosome 6 workshop report. (1999) (41)
Use of the CDR® plus NACC FTLD in mild FTLD: Data from the ARTFL/LEFFTDS consortium (2019) (41)
A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy. (2015) (41)
Genetics of Alcoholism (1998) (41)
Knowledge gaps and research recommendations for essential tremor. (2016) (41)
Genetic research: who is at risk for alcoholism. (2010) (40)
DSM-5 cannabis use disorder: a phenotypic and genomic perspective. (2014) (40)
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis (2020) (40)
Root resorption associated with orthodontic force in IL-1Beta knockout mouse. (2004) (40)
Association of the calcium-sensing receptor gene with blood pressure and urinary calcium in African-Americans. (2009) (40)
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases (2020) (40)
Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease (2017) (40)
Identification of QTLs Influencing Alcohol Preference in the High Alcohol Preferring (HAP) and Low Alcohol Preferring (LAP) Mouse Lines (2006) (39)
Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October 14-18, 1999. (2000) (39)
Structures of α-synuclein filaments from human brains with Lewy pathology (2022) (39)
Rarity of the Alzheimer disease-protective APP A673T variant in the United States. (2015) (39)
Parkinson's disease biomarkers: perspective from the NINDS Parkinson's Disease Biomarkers Program. (2017) (39)
Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men. (2005) (38)
Genome‐wide association studies of alcohol dependence, DSM‐IV criterion count and individual criteria (2019) (38)
Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees. (2002) (38)
Association of plasma and cortical amyloid beta is modulated by APOE ε4 status (2014) (38)
Clinical and Dopamine Transporter Imaging Characteristics of Leucine Rich Repeat Kinase 2 (LRRK2) and Glucosylceramidase Beta (GBA) Parkinson's Disease Participants in the Parkinson's Progression Markers Initiative: A Cross‐Sectional Study (2020) (38)
Genetics of Parkinson disease (2007) (38)
Clinical correlates of depressive symptoms in familial Parkinson's disease (2008) (37)
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms (2016) (37)
Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At‐Risk Individuals (2015) (37)
Linkage mapping of beta 2 EEG waves via non‐parametric regression (2003) (37)
Visual perception in prediagnostic and early stage Huntington's disease (2008) (36)
Saccadic eye movements are associated with a family history of alcoholism at baseline and after exposure to alcohol. (2002) (36)
Evolution of Alzheimer's Disease Cerebrospinal Fluid Biomarkers in Early Parkinson's Disease (2020) (36)
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease (2004) (36)
Genome Wide Linkage Analysis of 972 Bipolar Pedigrees Using Single Nucleotide Polymorphisms (2011) (35)
Predicting Short-term MCI-to-AD Progression Using Imaging, CSF, Genetic Factors, Cognitive Resilience, and Demographics (2019) (35)
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. (2015) (34)
Comprehensive gene- and pathway-based analysis of depressive symptoms in older adults. (2015) (34)
Genomewide association study identifies a novel locus for cannabis dependence (2017) (34)
Reliability of reported age at onset for Parkinson's disease (2003) (34)
Large-scale genomics unveil polygenic architecture of human cortical surface area (2015) (34)
G2019S mutation in the leucine‐rich repeat kinase 2 gene is not associated with multiple system atrophy (2007) (34)
Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study (2013) (34)
No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample (2005) (34)
Automatic Prediction of Conversion from Mild Cognitive Impairment to Probable Alzheimer's Disease using Structural Magnetic Resonance Imaging. (2010) (34)
Detection of Dental Fluorosis-Associated Quantitative Trait Loci on Mouse Chromosomes 2 and 11 (2008) (34)
Are Cognitive Changes Progressive in Prediagnostic HD? (2007) (34)
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk (2016) (33)
FASTKD2 is associated with memory and hippocampal structure in older adults (2014) (33)
Whole‐Genome Scan for Linkage to Bone Strength and Structure in Inbred Fischer 344 and Lewis Rats (2005) (33)
Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking (2013) (33)
A primary linkage map of the human chromosome 11q22-23 region. (1990) (33)
LRRK2: both a cause and a risk factor for Parkinson disease? (2005) (33)
Charcot-Marie-Tooth gene, SBF2, associated with taxane-induced peripheral neuropathy in African Americans (2016) (32)
Common genetic determinants of vitamin D insufficiency (2011) (32)
Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes. (2005) (32)
Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease (2006) (32)
An ADH1B variant and peer drinking in progression to adolescent drinking milestones: evidence of a gene-by-environment interaction. (2014) (32)
Heritability of Changes in Bone Size and Bone Mass With Age in Premenopausal White Sisters (2006) (31)
Defining Alcohol-Related Phenotypes in Humans (2002) (31)
Harnessing peripheral DNA methylation differences in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) to reveal novel biomarkers of disease (2020) (31)
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion. (1997) (31)
Association of TREM2 variants with Alzheimer's disease in African-Americans: For the Alzheimer's Disease Genetics Consortium (ADGC) (2013) (31)
Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration (2019) (31)
Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13. (2002) (30)
The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology (2019) (30)
From QTL to candidate gene: a genetic approach to alcoholism research. (2009) (30)
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. (1992) (30)
Genome screen in familial intracranial aneurysm (2009) (30)
Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking (2012) (29)
Genes influencing Parkinson disease onset (2004) (29)
Combined Face–Brain Morphology and Associated Neurocognitive Correlates in Fetal Alcohol Spectrum Disorders (2018) (29)
Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. (2014) (29)
Test-retest reliability of saccadic measures in subjects at risk for Huntington disease. (2009) (28)
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23. (2018) (28)
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide (2017) (28)
Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits (2016) (28)
Heterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility. (2011) (27)
Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength. (2006) (27)
Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci. (2009) (27)
Dopamine transporter imaging predicts clinically‐defined α‐synucleinopathy in REM sleep behavior disorder (2020) (27)
Brief Report: Genetics of Alcoholic Cirrhosis—GenomALC Multinational Study (2015) (27)
Inheritance of susceptibility to root resorption associated with orthodontic force in mice. (2008) (27)
Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4) (2018) (27)
Comparison of vertical and horizontal saccade measures and their relation to gray matter changes in premanifest and manifest Huntington disease (2012) (26)
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (26)
Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium. (1991) (26)
Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains (2005) (26)
Analyses of quantitative trait loci contributing to alcohol preference in HAD1/LAD1 and HAD2/LAD2 rats. (2003) (26)
Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration (2021) (26)
Women can bear a bigger burden: ante- and post-mortem evidence for reserve in the face of tau (2020) (26)
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease (2010) (26)
An endophenotype approach to the genetics of alcohol dependence: a genome wide association study of fast beta EEG in families of African ancestry (2017) (25)
Accelerated functional brain aging in pre-clinical familial Alzheimer’s disease (2021) (25)
Subjective perceptions associated with the ascending and descending slopes of breath alcohol exposure vary with recent drinking history. (2012) (25)
Absence of C9ORF72 expanded or intermediate repeats in autopsy‐confirmed Parkinson's disease (2014) (25)
Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration (2019) (25)
Genomes and phenomes of a population of outbred rats and its progenitors (2014) (25)
Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity (2017) (25)
Relation over time between facial measurements and cognitive outcomes in fetal alcohol-exposed children. (2012) (24)
Glutathione S-transferase 8-8 expression is lower in alcohol-preferring than in alcohol-nonpreferring rats. (2004) (24)
Genome‐wide Association Study and Meta‐analysis on Alcohol‐Associated Liver Cirrhosis Identifies Genetic Risk Factors (2020) (24)
Spheroid body myopathy revisited (1997) (24)
False Positive Rates in Association Studies as a Function of Degree of Stratification (2004) (24)
Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer’s disease (2017) (24)
Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease (2015) (24)
Impact of Genetic Ancestry on Outcomes in ECOG-ACRIN-E5103. (2017) (23)
Genetic and Neurophysiological Correlates of the Age of Onset of Alcohol Use Disorders in Adolescents and Young Adults (2013) (23)
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease (2016) (23)
TREM 2 is associated with increased risk for Alzheimer ' s disease in African Americans (23)
Family-based association analysis of alcohol dependence criteria and severity. (2014) (23)
A principal components analysis of the abbreviated Desires for Alcohol Questionnaire (DAQ). (2010) (23)
Expression Profiling and QTL Analysis: a Powerful Complementary Strategy in Drug Abuse Research (2005) (23)
Genetic architecture of age-related cognitive decline in African Americans (2016) (22)
Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice. (2009) (22)
Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales. (2002) (22)
Common biological networks underlie genetic risk for alcoholism in African‐ and European‐American populations (2013) (22)
Replication of Previous Genome-wide Association Studies of Bone Mineral Density in Premenopausal American Women (2010) (22)
Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer’s disease (2016) (22)
Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohort (2020) (22)
Development of Congenic Rat Strains for Alcohol Consumption Derived from the Alcohol-Preferring and Nonpreferring Rats (2006) (21)
18F-florbetapir Positron Emission Tomography–determined Cerebral &bgr;-Amyloid Deposition and Neurocognitive Performance after Cardiac Surgery (2018) (21)
A sex-adjusted and age-adjusted genome screen for nested alcohol dependence diagnoses (2005) (21)
Genome Screen to Detect Linkage to Common Susceptibility Genes for Intracranial and Aortic Aneurysms (2009) (21)
Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders (2019) (21)
Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure (2017) (21)
Confirmation of alcohol preference quantitative trait loci in the replicate high alcohol drinking and low alcohol drinking rat lines (2003) (20)
Genetics and Alcoholism: The COGA Project (2001) (20)
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms (2016) (20)
Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats. (2010) (20)
Clinical implications of gene discovery in Parkinson's disease and parkinsonism (2010) (20)
Adaptation of Subjective Responses to Alcohol is Affected by an Interaction of GABRA2 Genotype and Recent Drinking. (2015) (20)
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder (2016) (20)
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease (2018) (20)
Alpha‐synuclein and familial Parkinson's disease (2009) (20)
Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies (2019) (20)
Mapping of QTL Influencing Saccharin Consumption in the Selectively Bred Alcohol-Preferring and -Nonpreferring Rat Lines (2002) (19)
Calcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis. (2017) (19)
A Novel Joint Brain Network Analysis Using Longitudinal Alzheimer’s Disease Data (2019) (19)
Alcohol-preferring rats show decreased corticotropin-releasing hormone-2 receptor expression and differences in HPA activation compared to alcohol-nonpreferring rats. (2014) (19)
KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease (2021) (19)
Ethanol treatment of lymphoblastoid cell lines from alcoholics and non-alcoholics causes many subtle changes in gene expression. (2014) (19)
regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions (2012) (19)
Plasma Total-Tau and Neurofilament Light Chain as Diagnostic Biomarkers of Alzheimer's Disease Dementia and Mild Cognitive Impairment in Adults with Down Syndrome. (2020) (18)
Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint (2019) (18)
Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases (2021) (18)
Cis-Regulatory Variants Affect CHRNA5 mRNA Expression in Populations of African and European Ancestry (2013) (18)
Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint (2019) (18)
A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers. (2021) (18)
Copy Number Variation Accuracy in Genome-Wide Association Studies (2011) (18)
Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures (2016) (18)
Rates of lobar atrophy in asymptomatic MAPT mutation carriers (2019) (18)
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls (2019) (18)
Longitudinal Measurements of Glucocerebrosidase activity in Parkinson’s patients (2020) (17)
Genome-Wide Association Identifies the First Risk Loci for Psychosis in Alzheimer Disease (2020) (17)
Genome‐wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology (2020) (17)
The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala. (2002) (17)
Genetics of alcoholism. (2014) (17)
Linkage of type II and type III cystinuria to 19q13.1: codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone-forming phenotype. (1999) (17)
Implementation of a shared data repository and common data dictionary for fetal alcohol spectrum disorders research. (2010) (17)
Measurement invariance of DSM-IV alcohol, marijuana and cocaine dependence between community-sampled and clinically overselected studies. (2013) (17)
Plasma phosphorylated-tau181 as a predictive biomarker for Alzheimer’s amyloid, tau and FDG PET status (2021) (16)
The Longitudinal Early‐onset Alzheimer's Disease Study (LEADS): Framework and methodology (2021) (16)
Meta‐Analysis of Genetic Influences on Initial Alcohol Sensitivity (2018) (16)
Obesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk Drinkers. (2020) (16)
Plasma phosphorylated-tau181 as a predictive biomarker for Alzheimer’s amyloid, tau and FDG PET status (2021) (16)
Ondansetron blocks wild-type and p.F503L variant small-conductance Ca2+-activated K+ channels. (2018) (16)
Genome screen for platelet monoamine oxidase (MAO) activity. (1999) (16)
Allelic‐based gene‐gene interaction associated with quantitative traits (2009) (16)
A multivariate finite mixture latent trajectory model with application to dementia studies (2015) (16)
Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20 (2008) (16)
A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration (2020) (15)
Persistent changes in stress-regulatory genes in pregnant woman or a child with prenatal alcohol exposure. (2019) (15)
A Variant in XPNPEP 2 Is Associated with Angioedema Induced by Angiotensin I – Converting Enzyme Inhibitors (2005) (15)
Locus heterogeneity of autosomal dominant osteopetrosis (ADO). (1999) (15)
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease (2021) (15)
Novel recruitment strategy to enrich for LRRK2 mutation carriers (2015) (15)
Age at intracranial aneurysm rupture among generations (2009) (15)
Collagen COL22A1 maintains vascular stability and mutations in COL22A1 are potentially associated with intracranial aneurysms (2018) (15)
Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families (2012) (15)
Stoppage: An issue for segregation analysis (2001) (15)
Abnormal error-related antisaccade activation in premanifest and early manifest Huntington disease. (2011) (15)
Association of Adenylate Cyclase 10 (ADCY10) Polymorphisms and Bone Mineral Density in Healthy Adults (2009) (15)
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders (2018) (15)
Alzheimer's Disease Sequencing Project discovery and replication criteria for cases and controls: Data from a community-based prospective cohort study with autopsy follow-up (2017) (15)
Familial Intracranial Aneurysms: Is Anatomic Vulnerability Heritable? (2013) (15)
Nonlinear Z-score modeling for improved detection of cognitive abnormality (2019) (14)
Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1 (2012) (14)
Proteomic profiles for Alzheimer's disease and mild cognitive impairment among adults with Down syndrome spanning serum and plasma: An Alzheimer's Biomarker Consortium–Down Syndrome (ABC–DS) study (2020) (14)
Polygenic contributions to alcohol use and alcohol use disorders across population-based and clinically ascertained samples (2020) (14)
Affected Twins in the Familial Intracranial Aneurysm Study (2015) (14)
Feasibility and Safety of Multicenter Tissue and Biofluid Sampling for α-Synuclein in Parkinson’s Disease: The Systemic Synuclein Sampling Study (S4) (2018) (14)
Assessment of Blood Biomarker Profile After Acute Concussion During Combative Training Among US Military Cadets (2021) (13)
Epistatic Effects Contribute to Variation in BMD in Fischer 344 × Lewis F2 Rats (2007) (13)
Evaluation of laboratory tests for cirrhosis and for alcohol use, in the context of alcoholic cirrhosis. (2018) (13)
Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women (2006) (13)
Genes associated with alcohol outcomes show enrichment of effects with broad externalizing and impulsivity phenotypes in an independent sample. (2015) (13)
Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers (2019) (13)
Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond (2021) (13)
Differentially expressed genes strongly correlated with femur strength in rats. (2009) (13)
Polygenic risk for anxiety influences anxiety comorbidity and suicidal behavior in bipolar disorder (2020) (13)
Visual function in Huntington's disease patients and presymptomatic gene carriers (2003) (13)
Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck. (2008) (13)
Sex‐Specific Genetic Loci for Femoral Neck Bone Mass and Strength Identified in Inbred COP and DA Rats (2008) (13)
Visual scanning and cognitive performance in prediagnostic and early‐stage Huntington's disease (2009) (13)
Genome-wide analysis reveals novel genes in fl uencing temporal lobe structure with relevance to neurodegeneration in Alzheimer ' s disease (2010) (12)
Predicting alcohol use disorder remission: a longitudinal multimodal multi-featured machine learning approach (2021) (12)
Association studies of ALOX5 and bone mineral density in healthy adults (2008) (12)
Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI). (2019) (12)
Introduction to genetic linkage analysis. (1997) (12)
A semi-mechanism approach based on MRI and proteomics for prediction of conversion from mild cognitive impairment to Alzheimer’s disease (2016) (12)
Brain volumetric deficits in MAPT mutation carriers: a multisite study (2020) (12)
Staging tau pathology with tau PET in Alzheimer’s disease: a longitudinal study (2021) (12)
Staging tau pathology with tau PET in Alzheimer’s disease: a longitudinal study (2021) (12)
Fine Mapping Quantitative Trait Loci that Influence Alcohol Preference Behavior in the High and Low Alcohol Preferring (HAP and LAP) Mice (2011) (12)
Genome‐wide association studies of the self‐rating of effects of ethanol (SRE) (2019) (12)
Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population (2018) (11)
Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer’s disease families (2015) (11)
Cross-Sectional Exploration of Plasma Biomarkers of Alzheimer’s Disease in Down Syndrome: Early Data from the Longitudinal Investigation for Enhancing Down Syndrome Research (LIFE-DSR) Study (2021) (11)
Assessing the Genetic Risk for Alcohol Use Disorders (2012) (11)
Genetic loci affecting bone structure and strength in inbred COP and DA rats. (2008) (11)
The social symbiome framework: Linking genes-to-global cultures in public health using network science (2016) (11)
L1 coupling to ankyrin and the spectrin‐actin cytoskeleton modulates ethanol inhibition of L1 adhesion and ethanol teratogenesis (2018) (11)
Whole exome sequencing of intracranial aneurysm. (2013) (11)
Telomere Shortening in the Alzheimer's Disease Neuroimaging Initiative Cohort. (2019) (11)
A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior (2019) (11)
Association of Single Nucleotide Polymorphisms in a Glutamate Receptor Gene ( GRM 8 ) With Theta Power of Event-Related Oscillations and Alcohol Dependence (2008) (11)
Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians. (2015) (10)
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche DTU Orbit (05/11/2017) (2014) (10)
Genetics and Genomics of Late-Onset Alzheimer's Disease and Its Endophenotypes (2011) (10)
Association of Polygenic Liability for Alcohol Dependence and EEG Connectivity in Adolescence and Young Adulthood (2019) (10)
Biomarkers of neurodegeneration and glial activation validated in Alzheimer’s disease assessed in longitudinal cerebrospinal fluid samples of Parkinson’s disease (2021) (10)
Characteristics of Bipolar I patients grouped by externalizing disorders. (2015) (10)
SIBLING family genes and bone mineral density: association and allele-specific expression in humans. (2014) (10)
Interactive feature visualization and detection for 3D face classification (2010) (9)
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation (2007) (9)
Role of Lysosomal Gene Variants in Modulating GBA ‐Associated Parkinson's Disease Risk (2022) (9)
Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth (2016) (9)
FAM222A encodes a protein which accumulates in plaques in Alzheimer’s disease (2020) (9)
Genome‐wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward‐related ventral striatum activity in African‐ and European‐Americans (2019) (9)
Genes influencing spinal bone mineral density in inbred F344, LEW, COP, and DA rats (2010) (9)
Fine mapping of bone structure and strength QTLs in heterogeneous stock rat. (2015) (9)
Amyloid-associated increases in soluble tau relate to tau aggregation rates and cognitive decline in early Alzheimer’s disease (2022) (9)
RNA sequencing of whole blood reveals early alterations in immune cells and gene expression in Parkinson’s disease (2021) (9)
High‐Resolution Genome Screen for Bone Mineral Density in Heterogeneous Stock Rat (2014) (8)
Genomewide scan of affected relative pairs using the NIMH Genetics Initiative Bipolar affective Disorder pedigrees (1998) (8)
Chromosome 6 workshop. (1998) (8)
Recognition memory and divergent cognitive profiles in prodromal genetic frontotemporal dementia (2021) (8)
A genome wide association study of fast beta EEG in families of European ancestry. (2017) (8)
Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis (2019) (8)
Genomewide linkage study of modifiers of LRRK2‐related Parkinson's disease (2011) (8)
A telescope GWAS analysis strategy, based on SNPs-genes-pathways ensamble and on multivariate algorithms, to characterize late onset Alzheimer’s disease (2020) (8)
Genomes and phenomes of a population of outbred rats and its progenitors (2014) (8)
The commercial genetic testing landscape for Parkinson's disease. (2021) (8)
Translational research on aging: clinical epidemiology as a bridge between the sciences. (2014) (8)
Linkage Screen for BMD Phenotypes in Male and Female COP and DA Rat Strains (2008) (8)
Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants (2014) (8)
Genetic Testing for Parkinson Disease: Are We Ready? (2020) (7)
Epistasis between QTLs for bone density variation in Copenhagen × dark agouti F2 rats (2009) (7)
Identification of a Linkage Disequilibrium Block in Chromosome 1q Associated With BMD in Premenopausal White Women (2008) (7)
Correlation between Alzheimer’s disease and type 2 diabetes using non-negative matrix factorization (2021) (7)
Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics (2018) (7)
A Framework for 3D Analysis of Facial Morphology in Fetal Alcohol Syndrome (2010) (7)
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture (2020) (7)
Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort (2020) (7)
Linkage for platelet monoamine oxidase (MAO) activity: results from a replication sample. (2002) (7)
Genetic Research (2010) (6)
Understanding the Effects of Prenatal Alcohol Exposure Using Three Dimensional Facial Imaging (2011) (6)
A GABRA2 polymorphism improves a model for prediction of drinking initiation. (2017) (6)
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder (2019) (6)
Angiotensin-related genetic determinants of cardiovascular disease in patients undergoing hemodialysis. (2018) (6)
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) (2011) (6)
Dissociation of tau pathology and neuronal hypometabolism within the ATN framework of Alzheimer’s disease (2022) (6)
Genomewide Search forGenesInfluencing Percent BodyFatinPima Indians: Suggestive Linkage atChromosome 11q21-q22 (1997) (6)
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study (2020) (6)
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference (2018) (6)
Evaluating risk for alcohol use disorder: Polygenic risk scores and family history. (2022) (6)
Comprehensive analysis of epigenetic clocks reveals associations between disproportionate biological ageing and hippocampal volume (2022) (6)
Predicting Alzheimer’s disease progression using multi-modal deep learning approach (2019) (6)
20 cM genome scan of the NIMH Genetics Initiative Bipolar Pedigrees: chromosomes 1, 6, 8, 10 and 12 (1996) (6)
The association of polygenic risk for schizophrenia, bipolar disorder, and depression with neural connectivity in adolescents and young adults: examining developmental and sex differences (2021) (6)
Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance (2019) (6)
Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk (2021) (5)
CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men. (2008) (5)
Human and Animal Studies of the Genetics of Osteoporosis (2003) (5)
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-ε4 in female patients with Alzheimer’s disease (2022) (5)
DNA METHYLATION DYNAMICS IN ALZHEIMER’S DISEASE DIAGNOSIS AND PROGRESSION (2017) (5)
LRRK2 MUTATION ANALYSIS IN PARKINSON DISEASE FAMILIES WITH EVIDENCE OF LINKAGE TO PARKS. Authors' reply (2008) (5)
The BIN1 rs744373 SNP is associated with increased tau-PET levels and impaired memory (2019) (5)
A novel non‐parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib‐pairs (2008) (5)
Identification of genes for complex disease using longitudinal phenotypes (2003) (5)
Chromosome 5 and Parkinson disease (2006) (5)
Comprehensive cross-sectional and longitudinal analyses of plasma neurofilament light across FTD spectrum disorders (2022) (5)
Temporal order of clinical and biomarker changes in familial frontotemporal dementia (2022) (4)
Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90 (2022) (4)
Cross-Sectional and Longitudinal Validation of Serum Neurofilament Light Chain (NfL) as a Biomarker of Parkinson’s Disease Progression (2019) (4)
Quantitative trait locus for body weight identified on rat chromosome 4 in inbred alcohol-preferring and -nonpreferring rats: potential implications for neuropeptide Y and corticotrophin releasing hormone 2. (2013) (4)
Complex Genetics of Alcoholism (2014) (4)
The NIA Genetics of Alzheimer's Disease Data Storage Site (NIAGADS) (2012) (4)
ASLPrep: a platform for processing of arterial spin labeled MRI and quantification of regional brain perfusion (2022) (4)
Hippocampal-subfield microstructures and their relation to plasma biomarkers in Alzheimer's disease. (2022) (4)
Editorial: The genetics of absorptive hypercalciuria - A note of caution (2002) (4)
The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor’s Perspective (2018) (4)
The Genetics of Dementia (2013) (4)
Protein phosphatase 2A and complement component 4 are linked to the protective effect of APOE ɛ2 for Alzheimer's disease (2022) (4)
The genetics of absorptive hypercalciuria--a note of caution. (2002) (4)
Genome‐wide admixture mapping of DSM‐IV alcohol dependence, criterion count, and the self‐rating of the effects of ethanol in African American populations (2020) (4)
Meta‐Analyses of Externalizing Disorders: Genetics or Prenatal Alcohol Exposure? (2018) (4)
Association of plasma and cortical beta-amyloid is modulated by APOE ε4 status. (2014) (4)
Correction for Schumann et al., Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (3)
Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology (2020) (3)
Evidence for a susceptibility locus for bipolar disorder on chromosome 11p11.5 (1998) (3)
ERRATUM: Genome‐wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward‐related ventral striatum activity in African‐ and European‐Americans (2019) (3)
Longitudinal Analysis of Multiple Neurotransmitter Metabolites in Cerebrospinal Fluid in Early Parkinson's Disease (2021) (3)
NATIONAL CELL REPOSITORY FOR ALZHEIMER’S DISEASE: A BIOREPOSITORY FOR ALZHEIMER’S DISEASE AND RELATED DEMENTIA STUDIES (2018) (3)
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled Analysis (2022) (3)
Cryo-EM structures of α-synuclein filaments from Parkinson’s disease and dementia with Lewy bodies (2022) (3)
Alcoholism and mania: Is there a genetic relationship? (2001) (3)
Exome-chip association analysis of intracranial aneurysms (2019) (3)
Functional brain architecture is associated with the rate of tau accumulation in Alzheimer’s disease (2020) (3)
Genetic nurture effects for alcohol use disorder (2022) (3)
Replicating genetic linkage in the collaborative study on the genetics of alcoholism (COGA) (1998) (3)
Allele-Specific Expression and High-Throughput Reporter Assay Reveal Functional Variants in Human Brains with Alcohol Use Disorders (2019) (3)
Glucose metabolism patterns: A potential index to characterize brain ageing and predict high conversion risk into cognitive impairment (2022) (3)
Harnessing peripheral DNA methylation differences in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) to reveal novel biomarkers of disease (2020) (2)
Genetic findings using ADNI multimodal quantitative phenotypes: A 2014 update (2015) (2)
NONLINEAR N-SCORE ESTIMATION FOR ESTABLISHING COGNITIVE NORMS FROM THE NATIONAL ALZHEIMER’S COORDINATING CENTER (NACC) DATASET (2018) (2)
Sex‐associated differences in pathology burden in early‐onset Alzheimer’s disease (2020) (2)
The Alzheimer’s disease sequencing project–follow up study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer’s genetics research with addition of potential new cohorts (2020) (2)
Absence of C 9 ORF 72 expanded or intermediate repeats in autopsy confirmed Parkinson Disease (2014) (2)
A Genome-Wide Study of Familial Alzheimer’s Disease Supports Additional Candidate Genes: The NIA-LOAD/NCRAD Family Study (2011) (2)
Comparison of amyloid burden in individuals with Down syndrome versus autosomal dominant Alzheimer's disease: a cross-sectional study (2023) (2)
Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans (2022) (2)
Age-Specific Incidence Rate For Dementia And Alzheimer’s Disease In NIA-LOAD/NCRAD and EFIGA Families (P2.148) (2014) (2)
transcription factor NF-κB, with Alcohol Dependence (2007) (2)
Longitudinal clinical and biomarker characteristics of non-manifesting LRRK2 G2019S carriers in the PPMI cohort (2022) (2)
Longitudinal clinical and biomarker characteristics of non-manifesting LRRK2 G2019S carriers in the PPMI cohort (2022) (2)
Influence of rare reelin variants on quantitative PET imaging and CSF phenotypes in late-onset Alzheimer’s disease (2015) (2)
Genetic variation in PLXNA4 associated with susceptibility of Alzheimer’s disease through tau phosphorylation (2013) (2)
Use of Variable Marker Density, Principal Components, and Neural Networks in the Dissection of Disease Etiology (2001) (2)
Genetic variants in the SHISA6 gene are associated with delayed cognitive impairment in two family datasets (2021) (2)
Protein phosphatase 2A, complement component 4, and APOE genotype linked to Alzheimer disease using a systems biology approach (2020) (2)
Genome-wide rare variant analysis identifies candidate genes significantly associated with composite scores for memory (2015) (2)
Study in Parkinson’s disease of exercise phase 3 (SPARX3): study protocol for a randomized controlled trial (2022) (2)
Protein phosphatase 2A, complement component 4, and APOE genotype linked to Alzheimer’s disease using a systems biology approach (2020) (2)
Genome-wide association study of serum iron phenotypes in premenopausal women of European descent. (2016) (2)
Analysis of the Inverse Association between Cancer and Alzheimer’s Disease: Results from the Alzheimer’s Disease Neuroimaging Initiative Cohort (2014) (1)
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort (2023) (1)
Heritability of regional brain volumes in large-scale neuroimaging and genetic studies (2017) (1)
Relationship between CSF and plasma proteomic data in the ADNI-1 cohort (2012) (1)
FACIAL IMAGING CAN PROVIDE A MARKER FOR VERBAL PERFORMANCE DEFICITS IN CHILDREN WITH ALCOHOL-RELATED NEURODEVELOPMENTAL DISORDER (2014) (1)
Longitudinal Early‐onset Alzheimer’s Disease Study (LEADS) genetic screening: Initial results (2021) (1)
The National Institute on Aging Late‐Onset Alzheimer's Disease Family Based Study: A resource for genetic discovery (2022) (1)
Parametric Linkage Analysis and Disequilibrium Methods to Identify Loci for Complex Disease (2001) (1)
Association of Charcot-Marie-Tooth gene, SBF2, with taxane-induced peripheral neuropathy in African Americans. (2016) (1)
Haplotype Association Mapping In 33 Inbred Mouse Strains Identifies Genetic Regions Contributing To Chronic Hypoxia-Induced Pulmonary Hypertension (2012) (1)
Novel CYP1B1-RMDN2 Alzheimers disease locus identified by genome-wide association analysis of cerebral tau deposition on PET (2023) (1)
Genome-wide association study of CSF biomarkers amyloid beta 1-42, tau and tau phosphorylated at threonine 181 in the ADNI cohort (2010) (1)
Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease (2005) (1)
AMultiancestral Genome-Wide Exome Array Study of Alzheimer Disease , Frontotemporal Dementia , and Progressive Supranuclear Palsy (2015) (1)
Genetic Inheritance and Population Genetics (2008) (1)
Amyloid and tau PET in sporadic early‐onset Alzheimer’s disease: Preliminary results from LEADS (2020) (1)
The Alzheimer’s Disease Sequencing Project – Follow Up Study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer’s genetics research with the addition of potential new cohorts (2021) (1)
Characteristics and Progress on 312 Subjects in the Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects (LEFFTDS) Protocol (P3.036) (2018) (1)
A proteogenomic view of Parkinson’s disease causality and heterogeneity (2023) (1)
THE ALZHEIMER’S DISEASE SEQUENCING PROJECT (ADSP): DATA PRODUCTION, MANAGEMENT, AND AVAILABILITY (2016) (1)
Testing influences of APOE and BDNF genes and heart failure on cognitive function. (2020) (1)
ALZHEIMER’S DISEASE SEQUENCING PROJECT DISCOVERY AND REPLICATION CRITERIA FOR CASES AND CONTROLS: DATA FROM A COMMUNITY-BASED PROSPECTIVE COHORT STUDY WITH AUTOPSY FOLLOW-UP (2017) (1)
Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior (2017) (1)
Other Mutations: Their Role in Parkinson’s Disease (2004) (1)
Linkage of the indiana kindred variant of Gerstmann-Sträussler-Scheinker disease to a mutation in the prion protein gene ( PRNP ) (1992) (1)
TREM2 is associated with increased risk for Alzheimer’s disease in African Americans (2015) (1)
Assessment of heterogeneity among participants in the Parkinson's Progression Markers Initiative cohort using α-synuclein seed amplification: a cross-sectional study (2023) (1)
Alcoholism: Collaborative Study on the Genetics of Alcoholism (COGA) (2006) (1)
The Use of Linkage Data To Prioritize Results from Whole Exome Sequencing in Familial Intracranial Aneurysm (S53.001) (2012) (1)
The Asian Cohort for Alzheimer’s Disease (ACAD) study (2021) (1)
Preliminary analysis of copy number variation in the ADNI cohort (2010) (1)
IDENTIFICATION OF GENES UNDERLYING QTLS FOR ALCOHOL PREFERENCE IN ALCOHOL-PREFERRING AND -NONPREFERRING RATS. (2004) (1)
Genome-wide association study of stimulant dependence (2021) (1)
Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (1)
Test-Retest Reliability of Saccadic Measures (2009) (1)
Genome-wide SNP Linkage Screen for Intracranial Aneurysm Susceptibility Genes (2007) (1)
Abstract WMP26: Missense Mutation in COL22A1 is Associated With Intracranial Aneurysms (2016) (1)
PRIORITIZATION OF RESULTS FROM WHOLE EXOME SEQUENCING IN FAMILIAL INTRACRANIAL ANEURYSM (2012) (1)
Review Article Guidelines for the standardization of preanalytic variables for blood-based biomarker studies in Alzheimer's disease research (2014) (1)
Amplitude of Visual P3 Phenotypic Marker for a Event-Related Potential as a Predisposition to Alcoholism: Preliminary Results from the COGA Project (1998) (1)
Author Correction: Spread of pathological tau proteins through communicating neurons in human Alzheimer’s disease (2021) (1)
Can Salivary Innate Immune Molecules Provide Clue on Taste Dysfunction in COVID-19? (2021) (1)
CHARACTERISTICS AND PROGRESS ON THE INITIAL 209 SUBJECTS IN THE LONGITUDINAL EVALUATION OF FAMILIAL FRONTOTEMPORAL DEMENTIA SUBJECTS (LEFFTDS) PROTOCOL (2017) (1)
Studying the natural history of frontotemporal lobar degeneration (FTLD): The ARTFL LEFFTDS longitudinal FTLD (ALLFTD) protocol (2020) (0)
Author ' s personal copy Stress e response pathways are altered in the hippocampus of chronic alcoholics (2013) (0)
Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease (2018) (0)
Pairwise gene-protein association analysis on CSF proteomics in the ADNI-1 cohort (2012) (0)
SA137SOCIAL GENETICS EFFECTS ON ALCOHOL DEPENDENCE IN MARITAL DYADS (2019) (0)
Influence of rare RELN variants on quantitative PET imaging and CSF phenotypes in late-onset Alzheimer’s disease (2015) (0)
Exome Sequencing and Genomic Studies To Better Understand Alcohol Dependence (2019) (0)
Implementation of Blood‐Based Biomarker Assays to Deliver Consistent and Comparable Data (2022) (0)
VKučinskas-2001-2016 (2016) (0)
Genome-wide association study and admixture mapping of age-related cognitive decline in African-Americans (2013) (0)
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers (2013) (0)
PLASMA AMYLOID-BETA AND TAU AND VISUAL CONTRAST SENSITIVITY SYNERGISTICALLY PREDICT CEREBRAL AMYLOID AND TAU DEPOSITION ON PET IN PRECLINICAL AND PRODROMAL AD (2019) (0)
The Contribution of Known Familial Cardiovascular Disease Genes to Sudden Cardiac Death in Patients Undergoing Hemodialysis (2021) (0)
Genetic Data Identify Dual‐enrolled Participants in Alzheimer's Disease and Related Dementia (ADRD) Studies (2022) (0)
Neurodegeneration in the Longitudinal Evaluation of Early Onset Alzheimer’s Disease Study (LEADS) sample: Results from the MRI core (2020) (0)
Association of a locus on chromosome 17 with earlier age at onset of cognitive impairment in a familial Amish dataset (2021) (0)
Genome-wide linkage analyses of non-Hispanic White families identifies novel loci for familial late-onset Alzheimer ' s disease (2016) (0)
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks (2013) (0)
NEUROPATHOLOGY OF FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH A PRESENILIN 1 A396T MUTATION REVEALS THE COEXISTENCE OF Aβ, TAU, AND A-SYNUCLEIN PROTEINOPATHIES (2016) (0)
THE ALZHEIMER’S DISEASE SEQUENCING PROJECT (ADSP) DATA UPDATE 2018 (2018) (0)
Genetic and Neurophysiological Correlates of the Age of Onset of Alcohol Use Disorders in Adolescents and Young Adults (2013) (0)
Research Provides Direction in Ongoing Search for Genetic Links to Bipolar Disorder (2004) (0)
Erratum: Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus (Journal of Clinical Endocrinology and Metabolism 84 (4467-4471)) (2000) (0)
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2020) (0)
Clinical value of CSF tau, p‐tau181, neurogranin and neurofilaments in familial frontotemporal lobar degeneration (2021) (0)
Predicting Short-term MCI-to-AD Progression Using Imaging, CSF, Genetic Factors, Cognitive Resilience, and Demographics (2019) (0)
Demographic and psychosocial factors associated with the decision to learn mutation status in familial frontotemporal dementia and the impact of disclosure on mood (2021) (0)
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias (2023) (0)
Author Correction: FAM222A encodes a protein which accumulates in plaques in Alzheimer’s disease (2022) (0)
NEXT-GENERATION SEQUENCING OF THE BCHE LOCUS IDENTIFIES A FUNCTIONAL SNP ASSOCIATED WITH ALZHEIMER'S DISEASE BIOMARKERS AND AGE OF ONSET (2014) (0)
ADVANCING CLINICAL AND BIOMARKER RESEARCH IN AD: THE LEAD STUDY (2019) (0)
Comparison of C2N Diagnostics’ Aβ40, 42, and 42/40 ratio in Plasma Stored in Micronic and Sarstedt Tubes (2022) (0)
Genome-wide pathway analysis of memory impairment in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort implicates gene candidates, canonical pathways, and networks (2012) (0)
Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease. (2023) (0)
Frequency of Known Genetic Variants for Parkinson’s Disease in the PD GENEration Study Cohort (S42.002) (2023) (0)
O4‐04‐06: Withdrawn (2015) (0)
ADVANCING RESEARCH AND TREATMENT IN FRONTOTEMPORAL LOBAR DEGENERATION (ARTFL) NORTH AMERICAN RARE DISEASE CLINICAL RESEARCH CONSORTIUM: PROGRESS AND CHARACTERIZATION OF INITIAL PARTICIPANTS (2017) (0)
Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer’s disease (2016) (0)
GENE EXPRESSION OF ABCA7 DYSREGULATED IN PERIPHERAL BLOOD IS ASSOCIATED WITH DECREASED METABOLIC ACTIVITY IN HIPPOCAMPUS (2016) (0)
Deep learning-based polygenic risk analysis for Alzheimer’s disease prediction (2023) (0)
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
MULTIVARIATE PATTERNS OF ASSOCIATION BETWEEN DIFFUSION IMAGING METRICS AND PLASMA NEUROFILAMENT LIGHT IN PRODROMAL ALZHEIMER’S DISEASE (2019) (0)
Cognitive, neuropsychiatric and imaging comparisons between early‐onset and late‐onset Alzheimer’s disease participants from LEADS and ADNI3 (2021) (0)
Linkage of Pelizaeus-Merzbacher disease in a large family to the PLP region (1994) (0)
CHARACTERISTICS AND PROGRESS OF 320 SUBJECTS IN THE LONGITUDINAL EVALUATION OF FAMILIAL FRONTOTEMPORAL DEMENTIA SUBJECTS (LEFFTDS) PROTOCOL (2018) (0)
Edinburgh Research Explorer In Vivo Distribution of -Synuclein In Multiple Tissues and Biofluids in Parkinson’s Disease (0)
FRONTOTEMPORAL LOBAR DEGENERATION RESEARCH IN NORTH AMERICA: PROGRESS IN THE ARTFL/LEFFTDS CONSORTIA (2019) (0)
LRRK2 and GBA1 variant carriers have higher urinary bis(monacylglycerol) phosphate concentrations in PPMI cohorts (2023) (0)
Web‐based requisitioning, tracking and laboratory result reporting system for clinical trials using a central laboratory (2020) (0)
Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer’s disease (2017) (0)
THE ALZHEIMER’S DISEASE SEQUENCING PROJECT – FOLLOW UP STUDY (ADSP-FUS): INCREASING ETHNIC DIVERSITY IN ALZHEIMER’S GENETICS RESEARCH (2019) (0)
Gearing up for the future: Exploring facilitators and barriers to inform clinical trial design in frontotemporal lobar degeneration (2021) (0)
DIFFERENCES BETWEEN SPORADIC AND FAMILIAL BEHAVIORAL VARIANT FTD IN ADVANCING RESEARCH AND TREATMENT FOR FTLD (ARTFL) CLINICAL RESEARCH CONSORTIUM (2018) (0)
Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population (2018) (0)
' s response to reviews Title : Genome Screen in Familial Intracranial Aneurysm (2008) (0)
ANALYSING GENETIC AND TERATOGENIC EFFECTS OF ALCOHOL ON FACIAL FORM (2014) (0)
Genetic in fl uences on craving for alcohol (2012) (0)
Supporting Information Si Text Methods for Cohorts with Categorical Data on Alcohol Intake And (0)
Mutations disrupting PI3K signaling act as dominant enhancers of ethanol teratogenicity (2013) (0)
Linkage findings on chromosome 2 suggest a gene predisposing to multiple behavioral undercontrol phenotypes (2005) (0)
GENE MAP OF THE MSTD (MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA) REGION ON HUMAN CHROMOSOME 17q21–22 (1997) (0)
Pairwise gene-protein association analysis on cerebrospinal fluid proteomics in the ADNI-1 cohort (2012) (0)
APOE e4 status modulates the association of plasma and cortical Aβ: Relation of plasma Aβ and [11C]PiB PET in the ADNI cohort (2011) (0)
Linkage of Nedd4, a Regulator of the Epithelial Sodium Channel, to Primary Hypertension in Blacks (2000) (0)
P3-289: Apolipoprotein E and phosphodiesterase 4D variants associated with cognitive decline in elderly African-Americans (2008) (0)
Genome-wide association of plasma homocysteine in the indianapolis-ibadan dementia study cohort (2015) (0)
Diagnostic value of plasma phosphorylated tau181 in Alzheimer’s disease and frontotemporal lobar degeneration (2020) (0)
Reviewer Acknowledgment (2005) (0)
Age-specific incidence rates of Alzheimer's disease in family members participating in the NIA-LOAD genetics study (2013) (0)
Pattern Discovery in Brain Imaging Genetics via SCCA Modeling with a Generic Non-convex Penalty (2017) (0)
TYPE II CYSTINURIA LINKED TO 19q13.1 IN A FAMILY PEDIGREE (1999) (0)
241. The Collaborative Study of the genetics of alcoholism: Initial results and future goals (1998) (0)
Replication of suggestive linkage on chromosomes 5 and 16 in the NIMH genetics initiative bipolar pedigrees (2001) (0)
P3-247: Apolipoprotein E polymorphisms associated with risk of Alzheimer's disease in elderly African-Americans (2008) (0)
Association Studies of Neuropathologically-Confirmed Cases and Controls Reveals that the PARK10 Locus is a Major Contributor to Sporadic Parkinson disease. (S7.005) (2015) (0)
RARE VARIANT IN PLD3 IS ASSOCIATED WITH ALZHEIMER'S PATTERN OF NEURODEGENERATIVE CHANGES (2014) (0)
Sex and APOE‐ε4 carrier effects on early‐onset Alzheimer’s disease pathology (2022) (0)
Preliminary analysis of copy number variation in the ADNI cohort (2010) (0)
Diagnostic value of plasma P‐tau217 in frontotemporal dementia spectrum disorders (2021) (0)
Characteristic patterns of inter- and intra-hemispheric metabolic connectivity in patients with stable and progressive mild cognitive impairment and Alzheimer’s disease (2018) (0)
Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study (2020) (0)
enzyme-linked immunosorbent NONLINEAR N-SCORE ESTIMATION FOR ESTABLISHING COGNITIVE NORMS FROM (2018) (0)
THE MULTIDOMAIN IMPAIRMENT RATING (MIR) SCALE: INITIAL RELIABILITY DATA ON A MULTIDIMENSIONAL SCALE DESIGNED FOR FTLD SPECTRUM DISORDERS (2019) (0)
CLINICAL AND GENETIC PREDICTION OF ONSET AND COURSE OF ILLNESS IN SUBJECTS AT RISK FOR BIPOLAR DISORDER (2017) (0)
Binge and high‐intensity drinking—Associations with intravenous alcohol self‐administration and underlying risk factors (2022) (0)
Genetics of Addictive Disorders (2003) (0)
THE CLINICAL SPECTRUM OF FRONTOTEMPORAL LOBAR DEGENERATION IN NORTH AMERICA: BASELINE CHARACTERISTICS OF THE FIRST 912 PARTICIPANTS FROM THE ADVANCING RESEARCH AND TREATMENT IN FTLD (ARTFL) CLINICAL RESEARCH CONSORTIUM (2018) (0)
ASSOCIATION ANALYSIS OF RARE VARIANTS NEAR THE APOE REGION WITH CEREBROSPINAL FLUID (CSF) BIOMARKERS OF ALZHEIMER'S DISEASE (2014) (0)
The Asian Cohort for Alzheimer’s Disease (ACAD) Pilot Study (2022) (0)
GRAY MATTER DEFICITS IN SYMPTOMATIC AND PRESYMPTOMATIC MAPT MUTATION CARRIERS (2018) (0)
Influence of genetic variation on plasma proteomics in AD, MCI and controls: Pairwise gene-protein analysis in the ADNI-1 cohort (2011) (0)
P-175 Pleiotropic Effects of Novel Functional LRRK2 Variation on Crohn's Disease and Parkinson's Disease Risk (2016) (0)
O5-04-05 A NEW THERAPEUTIC STRATEGY FOR TAUOPATHIES: DISCOVERY OF HIGHLY POTENT BRAIN PENETRANT PROTAC DEGRADER MOLECULES THAT TARGET PATHOLOGIC TAU PROTEIN SPECIES (2019) (0)
Plasma biomarkers of inflammation reflect disease state in autosomal dominant forms of familial frontotemporal dementia (2020) (0)
Spread of pathological tau proteins through communicating neurons in human Alzheimer’s disease (2020) (0)
Mapping and characterization of structural variation in 17,795 human genomes (2020) (0)
Visual Scanning and Strategy in the Pre-Diagnostic and Early Stages of Huntington Disease (2008) (0)
Author Correction: Multimodal hippocampal subfield grading for Alzheimer’s disease classification (2020) (0)
Complement and NfL associations with brain structure and functional connectivity alterations in presymptomatic and symptomatic GRN mutation carriers (2021) (0)
Gene-based analyses of microglial activation on [11C]PBR28 PET in older adults at risk for Alzheimer's disease (2013) (0)
Oral Session II‐A (OII‐A) Special Populations 3:45 pm – 4:45 pm (2013) (0)
Multilocus genotype pattern at PICALM, CLU and APOE genes is associated with episodic memory in the NIA-LOAD/NCRAD study (2011) (0)
Replication and meta-analysis of the CHRFAM7A copy number variant in a cohort of clinically characterized and neuropathologically verified individuals (2012) (0)
Interpretation of Genetic Linkage Findings (2003) (0)
Identifying genetic risk factors for idiopathic Parkinson's disease by combining genome-wide copy number variation data and published data from genome-wide sib-pair linkage studies (2006) (0)
Integrating whole-exome sequencing and imaging genetics to identify single-nucleotide variants associated with rate of hippocampal neurodegeneration in APOE-ε3/ε3 males with mild cognitive impairment (2012) (0)
Author Correction: Multimodal hippocampal subfield grading for Alzheimer’s disease classification (2020) (0)
The role of APOE genotype in early mild cognitive impairment (E-MCI): Preliminary results from ADNI-2 (2012) (0)
A global view of the genetic basis of Alzheimer disease (2023) (0)
Detection of dental fluorosis associated QTL on mouse chromosomes 2 and 11 (2010) (0)
Cocaine Abuse Dependence Major depressive episode Current Lifetime Marijuana Abuse Dependence Mania Cunent Lifetime Obsessivekompulsive Opioid Abuse Dependence Panic disorder Sedative Abuse Dependence Somatization disorder Stimulant Abuse Deoendence (1998) (0)
DNA METHYLATION DYNAMICS IN ALZHEIMER’S DISEASE: DEVELOPMENT OF BIOMARKERS AND NOVEL DRUG TARGETS USING ADNI EPIGENETIC DATA (2018) (0)
GENETIC FINDINGS USING ADNI MULTIMODAL QUANTITATIVE PHENOTYPES: A REVIEW OF PAPERS PUBLISHED IN 2013 (2014) (0)
Common gene networks underlying memory impairment: A comparison of pathway analysis methods in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort (2012) (0)
FGF23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis (2019) (0)
Implementation of a Distributed Architecture for Managing Collection and Dissemination of Data for Fetal Alcohol Spectrum Disorders Research (2007) (0)
Genome-Wide SNP Linkage Screen for Intracranial Aneurysm Susceptibility Genes: Results from 333 Multiplex IA Families (2008) (0)
Plasma Neuro ﬁ lament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration (0)
Parkinson's Progression Markers Initiative brain autopsy program. (2022) (0)
P3‐013: Withdrawn (2015) (0)
LOSS OF Y CHROMOSOME: GENETICS AND ASSOCIATION WITH ALZHEIMER’S DISEASE ENDOPHENOTYPES (2019) (0)
Gene mapping using linkage analysis. (1991) (0)
The Social Symbiome Framework (2016) (0)
The National Institute on Aging Late Onset Alzheimer's Disease Family Based Study: A Critical Component of the International Effort to Understand Alzheimer's Disease (2021) (0)
MAPT haplotypes modify the association between head injury and risk of Alzheimer’s disease (2015) (0)
Replication and meta-analysis of the CHRFAM7A copy number variant in a cohort of clinically characterized and neuropathologically verified individuals (2012) (0)
84084 Team Science to maximize rapid collection and analyses of biosamples from patients with Covid-19 (2021) (0)
PLASMA AMYLOID-BETA AND TAU AND VISUAL CONTRAST SENSITIVITY SYNERGISTICALLY PREDICT CEREBRAL AMYLOID AND TAU DEPOSITION ON PET IN PRECLINICAL AND PRODROMAL AD (2019) (0)
Allele frequency heterogeneity in the collaborative study on the genetics of alcoholism (COGA) (2000) (0)
The role of APOE-ɛ4 genotype in early mild cognitive impairment (EMCI): Preliminary results from ADNI-2 (2012) (0)
USING A BRAIN NETWORK APPROACH TO PREDICT GENETIC MUTATION IN INDIVIDUAL PATIENTS WITH FAMILIAL FRONTOTEMPORAL DEMENTIA (2018) (0)
Associations of targeted genetic variants with Alzheimer’s disease in African Americans and Nigerians (2020) (0)
Gene expression profiling identifies altered networks in late-onset Alzheimer’s disease: Immune response and mitochondrial process (2015) (0)
The Advancing Research and Treatment in Frontotemporal Lobar Degeneration (ARTFL) North American Rare Disease Clinical Research Consortium: Progress and Participant Characterization (S2.008) (2018) (0)
Table 1. [Parkinson Disease: Molecular Genetics]. (2014) (0)
A review of published genetic studies using ADNI multimodality quantitative phenotypes: MRI, PET, fluid biomarkers, cognition and clinical status (2013) (0)
Acknowledgement to referees 2003 (2004) (0)
ADRC GWAS supplement: An NCRAD initiative (2021) (0)
AMYLOID NEUROIMAGING AND GENETICS INITIATIVE: A RESOURCE FOR INVESTIGATORS (2019) (0)
TRACKING WHITE MATTER DEGENERATION IN ASYMPTOMATIC AND SYMPTOMATIC MAPT MUTATION CARRIERS WITH DTI (2019) (0)
Transcriptome-guided neurogenesis gene pathway variation is associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease (2015) (0)
TREM2 Variants in Parkinson’s Disease: Results from the Parkinson’s Progression Markers Initiative (PPMI) Study (2022) (0)
Abbreviated Desires for Alcohol Questionnaire (2018) (0)
A review of published genetic studies using ADNI multimodality quantitative phenotypes: MRI, PET, fluid biomarkers, cognition and clinical status (2013) (0)
GENOME-WIDE META-ANALYSIS OF TRANSCRIPTOME PROFILING IDENTIFIES NOVEL DYSREGULATED GENES IMPLICATED IN ALZHEIMER’S DISEASE (2016) (0)
GENOME-WIDE LINKAGE ANALYSIS OF AFRICAN-AMERICAN ALZHEIMER DISEASE FAMILIES (2019) (0)
Protective variant for rate of hippocampal volume loss identified by whole exome sequencing in APOE-ε3ε3 males with MCI (2013) (0)
Relationship between CSF and plasma proteomic data in the ADNI-1 cohort (2012) (0)
NCRAD Family Study and NIA‐LOAD brain tissue: A NCRAD resource (2021) (0)
The trend of disruption in the functional brain network topology of Alzheimer’s disease (2021) (0)
Plasma neurofilament light chain levels reflect caregiver burden and social cognition measures in familial frontotemporal lobar degeneration (FTLD) (2020) (0)
Inflammatory profile in LRRK2-associated prodromal and clinical PD (2016) (0)
Higher CSF sTREM2 attenuates ApoE4-related risk for cognitive decline and neurodegeneration (2020) (0)
Title Polygenic risk for externalizing disorders : Gene-by-development and gene-by-environment effects in adolescents and young adults (2015) (0)
Gwas of longitudinal amyloid PET identifies IL1RAP as a new potential Alzheimer's disease target (2015) (0)
Erratum (2016) (0)
Amyloid pathway-based candidate gene analysis of [11C]PiB-PET in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort (2011) (0)
THE GROWTH AND IMPACT OF ADNI GENETICS PUBLICATIONS AS MEASURED BY SCIENCE MAPPING (2016) (0)
CTNNA3, CAPRIN2 and SPG20 are significantly associated with Alzheimer's disease in preliminary analyses of a genome-wide association study in African-Americans (2012) (0)
THE GROWTH AND IMPACT OF ADNI GENETICS PUBLICATIONS AS MEASURED BY SCIENCE MAPPING (2016) (0)
AMYLOID NEUROIMAGING AND GENETICS INITIATIVE: IMPLEMENTING DNA COLLECTION USING NOVEL CONSENTING APPROACHES FOR AN IDEAS ADD-ON STUDY (2018) (0)
Twelfth annual symposia on etiology, pathogenesis, and treatment of parkinson's disease and etiology, pathogenesis, and treatment of Huntington's disease (1998) (0)
Corrigendum to: 'A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers' [J Hepatol 2022 (76) 275-282]. (2022) (0)
Oculomotor Control in Parkinson’s Patients and Their Clinically Normal Siblings (2005) (0)
THE ALZHEIMER’S DISEASE SEQUENCING PROJECT (ADSP) DATA UPDATE 2017 (2017) (0)
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts (2015) (0)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (0)
GENOME-WIDE LINKAGE ANALYSES OF AFRICAN AMERICAN FAMILIES SUPPORTS EVIDENCE OF LINKAGE TO CHROMOSOME 12 (2018) (0)
ADSP follow‐up study: NCRAD biospecimens (2021) (0)
Gene-based analyses of microglial activation on [11C] PBR28 PET in older adults at risk for Alzheimer's disease (2013) (0)
GENETIC FINDINGS USING ADNI MULTIMODAL QUANTITATIVE PHENOTYPES: A REVIEW OF PAPERS PUBLISHED IN 2013 (2014) (0)
Predictors of memory performance in a large, stratified, random population sample of older Americans: Clinical, demographic, lifestyle and genetic factors (2013) (0)
The Alzheimer’s Disease Sequencing Project Follow Up Study (ADSP‐FUS): increasing ethnic diversity in Alzheimer’s disease (AD) genetics research. (2022) (0)
Genomewide Screen for Intracranial Aneurysm Susceptibility Genes (2006) (0)
Nonparametric linkage and family‐based association studies of a simulated complex disorder (1999) (0)
APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestry (2022) (0)
Establishing a centralized repository of human pluripotent stem cells for neurodegeneration research (2021) (0)
GENOME-WIDE META-ANALYSIS OF TRANSCRIPTOME PROFILING IDENTIFIES NOVEL DYSREGULATED GENES IMPLICATED IN ALZHEIMER’S DISEASE (2016) (0)
A multinational deployment of 3D laser scanning to study craniofacial dysmorphology in fetal alcohol spectrum disorders (2007) (0)
GENE EXPRESSION OF ABCA7 DYSREGULATED IN PERIPHERAL BLOOD IS ASSOCIATED WITH DECREASED METABOLIC ACTIVITY IN HIPPOCAMPUS (2016) (0)
Increased white matter MRI T1 hypointensity volume in young‐onset Alzheimer’s disease patients is not accounted for by age or cardiovascular risk factors (2020) (0)
INFLUENCE OF RARE PSEN1 VARIANTS ON QUANTITATIVE STRUCTURAL IMAGING AND CSF PHENOTYPES IN LATE ONSET ALZHEIMER'S DISEASE (2014) (0)
RARE VARIANT IN PLD3 IS ASSOCIATED WITH ALZHEIMER'S PATTERN OF NEURODEGENERATIVE CHANGES (2014) (0)

This paper list is powered by the following services:

Other Resources About Tatiana Foroud

en.wikipedia.org
medicine.iu.edu

What Schools Are Affiliated With Tatiana Foroud?

Tatiana Foroud is affiliated with the following schools:

Indiana University Bloomington
Indiana University
University of Sydney
Fairfield University
University of Eastern Finland
Indiana University–Purdue University Indianapolis
University of California, Los Angeles
Purdue University
Rush University
University of California, San Francisco