Ian W. Craig

Q: What Schools Are Affiliated With Ian W. Craig

Ian W. Craig is affiliated with the following schools: King's College London, King's College, Aberdeen, Queen's University Belfast, University of California, Berkeley, University of California, Santa Barbara, University of Oxford, Queen's University at Kingston, Queens University , Stanford University

Ian W. Craig's AcademicInfluence.com Rankings

Ian W. Craig

Computer Science

#5241

World Rank

#5535

Historical Rank

Computational Linguistics

#685

World Rank

#697

Historical Rank

Machine Learning

#1313

World Rank

#1333

Historical Rank

Artificial Intelligence

#1552

World Rank

#1581

Historical Rank

computer-science Degrees

Download Badge

Computer Science

Ian W. Craig's Degrees

PhD Computer Science Stanford University
Masters Computer Science University of California, Berkeley
Bachelors Computer Science University of California, Berkeley

Similar Degrees You Can Earn

Why Is Ian W. Craig Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Ian W. Craig'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

Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene (2003) (7618)
Role of Genotype in the Cycle of Violence in Maltreated Children (2002) (4368)
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)
Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
Letter abstract - Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's Disease (2009) (1644)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, and shows evidence for additional susceptibility genes (2009) (1441)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2013) (1388)
Moderation of the Effect of Adolescent-Onset Cannabis Use on Adult Psychosis by a Functional Polymorphism in the Catechol-O-Methyltransferase Gene: Longitudinal Evidence of a Gene X Environment Interaction (2005) (1279)
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease (2014) (1230)
MAOA, maltreatment, and gene–environment interaction predicting children's mental health: new evidence and a meta-analysis (2006) (1114)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (1073)
A mega-analysis of genome-wide association studies for major depressive disorder (2013) (979)
Gene–environment interaction analysis of serotonin system markers with adolescent depression (2004) (697)
A common molecular basis for three inherited kidney stone diseases (1996) (696)
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)
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2010) (587)
DNA Pooling: a tool for large-scale association studies (2002) (560)
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes (2006) (550)
Localization of the X inactivation centre on the human X chromosome in Xq13 (1991) (378)
Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism (2007) (377)
Statins for the prevention of dementia. (2009) (365)
Genome-wide association study of bipolar disorder in European American and African American individuals (2009) (354)
Expression of the dopamine transporter gene is regulated by the 3' UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR. (2002) (346)
Candidate Genes Expression Profile Associated with Antidepressants Response in the GENDEP Study: Differentiating between Baseline ‘Predictors' and Longitudinal ‘Targets' (2012) (330)
Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. (2010) (330)
A mutation in the Norrie disease gene (NDP) associated with X–linked familial exudative vitreoretinopathy (1993) (311)
A longitudinal study of epigenetic variation in twins (2010) (310)
Common variants at ABCA 7 , MS 4 A 6 A / MS 4 A 4 E , EPHA 1 , CD 33 and CD 2 AP are associated with Alzheimer ’ s disease (2011) (292)
Genome-wide association study of major recurrent depression in the U.K. population. (2010) (251)
Brain Monoamine Oxidase A Activity Predicts Trait Aggression (2008) (227)
Risk factors for dementia. (2001) (227)
Behavioral genetics in the postgenomic era (2003) (220)
Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies. (2013) (219)
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. (1985) (219)
The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression (2009) (211)
Statins for the treatment of dementia (2010) (206)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Genetic predictors of response to antidepressants in the GENDEP project (2009) (204)
A cross-sectional study of neuropsychiatric symptoms in 435 patients with Alzheimer's disease. (2005) (199)
Genetics of human aggressive behaviour (2009) (195)
Isolation and characterization of a candidate gene for Norrie disease (1992) (195)
A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample. (2006) (184)
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium☆ (2017) (183)
Genome-wide association study of CSF biomarkers Aβ1-42, t-tau, and p-tau181p in the ADNI cohort (2010) (175)
Polygenic interactions with environmental adversity in the aetiology of major depressive disorder (2015) (173)
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)
Singleton deletions throughout the genome increase risk of bipolar disorder (2009) (159)
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). (1994) (157)
Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays (2008) (156)
Regular Research ArticlesA Cross-Sectional Study of Neuropsychiatric Symptoms in 435 Patients With Alzheimer's Disease (2005) (154)
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. (1997) (149)
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). (1995) (148)
Behavioural and psychological syndromes in Alzheimer's disease (2004) (144)
Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol‐O‐methyltransferase (COMT) gene (2006) (144)
Moderation of antidepressant response by the serotonin transporter gene (2009) (143)
Dinucleotide repeat polymorphism at the MAOA locus. (1991) (136)
Association analysis of MAOA and COMT with neuroticism assessed by peers (2003) (135)
Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance (1981) (135)
Retinal microvascular network attenuation in Alzheimer's disease (2015) (132)
Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis. (1987) (129)
Muscular dystrophy in girls with X;autosome translocations. (1986) (128)
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease. (1989) (127)
Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships. (2004) (124)
The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression (2006) (123)
Genetic Predictors of Response to Serotonergic and Noradrenergic Antidepressants in Major Depressive Disorder: A Genome-Wide Analysis of Individual-Level Data and a Meta-Analysis (2012) (120)
Galantamine for vascular cognitive impairment. (2006) (120)
A retrospective study of the behavioural and psychological symptoms of mid and late phase Alzheimer's disease (2003) (118)
Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms (2011) (114)
The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression (2013) (113)
Evidence That Brain MAO A Activity Does Not Correspond to MAO A Genotype in Healthy Male Subjects (2007) (112)
Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome-wide association and polygenic scoring study (2014) (108)
The importance of stress and genetic variation in human aggression (2007) (108)
Prediction of heterogeneity in intelligence and adult prognosis by genetic polymorphisms in the dopamine system among children with attention-deficit/hyperactivity disorder: evidence from 2 birth cohorts. (2006) (107)
Functional effects of a tandem duplication polymorphism in the 5′flanking region of the DRD4 gene (2004) (106)
Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP‐25, and 5HT1B (2005) (106)
Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project (2010) (104)
Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression (2011) (103)
Genetic Predictors of Increase in Suicidal Ideation During Antidepressant Treatment in the GENDEP Project (2009) (103)
Genotyping Pooled DNA on Microarrays: A Systematic Genome Screen of Thousands of SNPs in Large Samples to Detect QTLs for Complex Traits (2004) (103)
Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children (2008) (103)
Localization of human tryptophan hydroxylase (TPH) to chromosome 11p15.3----p14 by in situ hybridization. (1991) (100)
SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children. (2005) (99)
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders (2015) (95)
Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1) (2005) (94)
DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. (1999) (93)
Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat (1999) (93)
A Genome-Wide Scan of 1842 DNA Markers for Allelic Associations with General Cognitive Ability: A Five-Stage Design Using DNA Pooling and Extreme Selected Groups (2001) (91)
The serotonin transporter gene as a QTL for ADHD (2005) (89)
Localization of the human dopamine beta hydroxylase (DBH) gene to chromosome 9q34. (1988) (88)
GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. (2000) (88)
The correlation between reading and mathematics ability at age twelve has a substantial genetic component (2014) (87)
Interaction between serotonin transporter gene variants and life events predicts response to antidepressants in the GENDEP project (2011) (87)
Depressive disorder moderates the effect of the FTO gene on body mass index (2012) (86)
Differential methylation of the X‐chromosome is a possible source of discordance for bipolar disorder female monozygotic twins (2008) (85)
Executive functioning in Alzheimer's disease and vascular dementia (2009) (80)
Rivastigmine for vascular cognitive impairment. (2013) (79)
Mutations in the Norrie disease gene (1995) (79)
The current state of play on the molecular genetics of depression (2012) (78)
Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22. (1989) (78)
Attention deficits in Alzheimer's disease and vascular dementia (2010) (77)
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. (1994) (76)
Stressful life events and the brain-derived neurotrophic factor gene in bipolar disorder. (2010) (76)
Tumor necrosis factor and its targets in the inflammatory cytokine pathway are identified as putative transcriptomic biomarkers for escitalopram response (2013) (76)
Functional polymorphisms in dopamine and serotonin pathway genes (2006) (75)
Genetic differences in cytochrome P450 enzymes and antidepressant treatment response (2014) (75)
Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif. (1992) (74)
Genotyping DNA pools on microarrays: Tackling the QTL problem of large samples and large numbers of SNPs (2005) (72)
Neural mechanisms of anger regulation as a function of genetic risk for violence. (2009) (71)
Cochrane review on ‘Statins for the treatment of dementia’ (2013) (70)
A HIGHLY INFORMATIVE X‐CHROMOSOME PROBE, M27β, CAN BE USED FOR THE DETERMINATION OF TUMOUR CLONALITY (1990) (70)
CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP (2012) (70)
Organization of the human monoamine oxidase genes and long-range physical mapping around them. (1992) (70)
A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD) (2011) (70)
Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]. (1987) (69)
The quest for quantitative trait loci associated with intelligence (2006) (69)
Pharmacogenetics of antidepressant response: A polygenic approach (2016) (69)
Structure of the human gene for monoamine oxidase type A. (1991) (68)
Statins for the prevention of dementia. (2016) (68)
Language-impaired children: No sign of the FOXP2 mutation (2002) (68)
Platelet β-secretase activity is increased in Alzheimer's disease (2008) (66)
No association with the 5,10‐methylenetetrahydrofolate reductase gene and major depressive disorder: Results of the depression case control (DeCC) study and a meta‐analysis (2008) (66)
Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies (2010) (66)
Genetically increased risk of sleep disruption in Alzheimer's disease. (2006) (66)
The genetics of affective disorder and suicide (2010) (66)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2009) (64)
A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. (2011) (64)
Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. (2009) (63)
A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds. (2005) (63)
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3. (1991) (62)
Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders (2014) (62)
Methyl‐CpG‐binding protein 2 polymorphisms and vulnerability to autism (2008) (62)
Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways. (1986) (62)
Candidate Genes Expression Profile Associated with Antidepressants Response in the GENDEP Study: Differentiating between Baseline ‘Predictors’ and Longitudinal ‘Targets’ (2013) (62)
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. (2012) (61)
DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for association (2005) (60)
P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? (2009) (57)
Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers (1995) (57)
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder (2015) (57)
Homologous expressed genes in the human sex chromosome pairing region (1985) (56)
Long-range chromosomal mapping of the carcinoembryonic antigen (CEA) gene family cluster. (1992) (56)
Concordant Association of Insulin Degrading Enzyme Gene (IDE) Variants with IDE mRNA, Aß, and Alzheimer's Disease (2010) (56)
Shared genetic contribution to ischemic stroke and Alzheimer's disease (2016) (55)
Apolipoprotein E e4 allele influences aggressive behaviour in Alzheimer’s disease (2004) (55)
A Genome-Wide Association Study of Social and Non-Social Autistic-Like Traits in the General Population Using Pooled DNA, 500 K SNP Microarrays and Both Community and Diagnosed Autism Replication Samples (2009) (53)
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case. (1995) (53)
Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies (2018) (53)
The Genetic Basis for Sex Differences in Human Behaviour: Role of the Sex Chromosomes (2004) (53)
Assignment of the haemophilia B (Factor IX) locus to the q26‐qter region of the X chromosome (1984) (52)
Report of the committee on the genetic constitution of chromosomes 12 and 13. (1989) (51)
Genome Wide Association Analysis of Copy Number Variation in Recurrent Depressive Disorder (2011) (51)
Genetics, environment and cognitive abilities: review and work in progress towards a genome scan for quantitative trait locus associations using DNA pooling. (2001) (51)
Variation in GNB3 predicts response and adverse reactions to antidepressants (2011) (51)
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene. (1992) (51)
Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms (2005) (50)
Epigenome-Wide Association Study for Parkinson’s Disease (2014) (50)
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals† (2017) (49)
Genetic Control of Mitochondrial Enzymes in Human–Mouse Somatic Cell Hybrids (1973) (49)
Functional genetic polymorphisms in serotonin and dopamine gene systems and their significance in behavioural disorders. (2008) (48)
Estimating the heritability of reporting stressful life events captured by common genetic variants (2012) (48)
CLOSE LINKAGE OF HYPERVARIABLE MARKER DXS255 TO DISEASE LOCUS OF WISKOTT-ALDRICH SYNDROME (1989) (47)
Genes within the serotonergic system are differentially expressed in human brain (2009) (46)
Interaction between specific forms of childhood maltreatment and the serotonin transporter gene (5-HTT) in recurrent depressive disorder. (2013) (46)
The development of effective biomarkers for Alzheimer's disease: a review (2013) (46)
Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain (2014) (44)
Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case–control study (BACCS) (2009) (44)
The dopamine D4 receptor and the hyperactivity phenotype: a developmental-epidemiological study (2002) (43)
Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe. (1991) (43)
The prevalence of age-related macular degeneration in Alzheimer's disease. (2010) (43)
Integrative mouse and human mRNA studies using WGCNA nominates novel candidate genes involved in the pathogenesis of major depressive disorder. (2013) (43)
Localisation of the Gγ-, Aγ-, δ- and β-globin genes on the short arm of human chromosome 11 (1979) (43)
A multi-center study of ACE and the risk of late-onset Alzheimer's disease. (2011) (42)
Molecular heterogeneity of translocations associated with muscular dystrophy (1987) (42)
Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa. (1990) (42)
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays (2005) (42)
A Longitudinal Twin Study of Skewed X Chromosome-Inactivation (2011) (42)
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3. (1992) (41)
Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene? (1987) (41)
Norrie disease gene: characterization of deletions and possible function. (1993) (41)
The future of memory clinics (2004) (41)
X inactivation as a source of behavioural differences in monozygotic female twins. (2004) (41)
A novel expression based approach for assessing the inactivation status of human X-linked genes (2000) (38)
A novel reciprocal and biphasic relationship between membrane cholesterol and β‐secretase activity in SH‐SY5Y cells and in human platelets (2009) (38)
New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation (2017) (38)
ABCA7 p.G215S as potential protective factor for Alzheimer's disease (2016) (38)
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp. (1997) (37)
CGM2, a member of the carcinoembryonic antigen gene family is down-regulated in colorectal carcinomas. (1994) (37)
Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes (2004) (36)
Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing (2018) (36)
Platelet beta-secretase activity is increased in Alzheimer's disease. (2008) (36)
Convergent Animal and Human Evidence Suggests a Role of PPM1A Gene in Response to Antidepressants (2011) (35)
Statins for the treatment of dementia. (2010) (35)
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease (2003) (34)
Human behavioural genetics of cognitive abilities and disabilities (1997) (34)
Genetic Variation in the α7 Nicotinic Acetylcholine Receptor is Associated with Delusional Symptoms in Alzheimer’s Disease (2008) (34)
Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint. (1996) (33)
Dissecting the Genetic Heterogeneity of Depression Through Age at Onset (2012) (33)
Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy. (1995) (33)
DNA pooling and dense marker maps: a systematic search for genes for cognitive ability. (1999) (33)
Neurobiology and genetics of behavioural syndromes of Alzheimer's disease. (2004) (33)
A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase locus. (1992) (32)
Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblings (2005) (32)
Association Analysis of Apolipoprotein E Genotype and Risk of Depressive Symptoms in Alzheimer’s Disease (2005) (31)
The Bipolar Association Case–Control Study (BACCS) and meta‐analysis: No association with the 5,10‐Methylenetetrahydrofolate reductase gene and bipolar disorder (2010) (31)
Exploring the role of drug-metabolising enzymes in antidepressant side effects (2015) (31)
Localisation of Y chromosome sequences in normal and 'XX' males. (1987) (31)
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3 (2018) (31)
Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy. (1988) (31)
Antidepressant-dependent mRNA changes in mouse associated with hippocampal neurogenesis in a mouse model of depression (2012) (30)
Hydrophobic Protein that Copurifies with Human Brain Acetylcholinesterase (2000) (30)
Characterization of a mutation within the NDP gene in a family with a manifesting female carrier. (1993) (30)
Alzheimer's disease and age-related macular degeneration have different genetic models for complement gene variation (2012) (30)
A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: A Preliminary Study (2014) (29)
Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2 (1992) (29)
Factors influencing prescription of CNS medications in different elderly populations (2003) (29)
α7 Nicotinic acetylcholine receptor gene and reduced risk of Alzheimer’s disease (2007) (29)
Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes (2012) (29)
Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq (1989) (28)
The interleukin 1β gene promoter polymorphism (−511) acts as a risk factor for psychosis in Alzheimer's dementia (2004) (28)
Assignment of the human tyrosine hydroxylase gene to chromosome 11 (1984) (28)
Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease (2018) (28)
Interaction between childhood maltreatment on immunogenetic risk in depression: Discovery and replication in clinical case-control samples (2018) (27)
Psychotic symptoms in Alzheimer’s disease are not influenced by polymorphic variation at the dopamine receptor DRD3 gene (2004) (27)
Analysis of the monoamine oxidase genes and the Norrie disease gene locus in narcolepsy (1999) (27)
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder (2016) (26)
AVPR1A and SLC6A4 Polymorphisms in Choral Singers and Non-Musicians: A Gene Association Study (2012) (26)
Genomic organization of human centromeric alpha satellite DNA: characterization of a chromosome 17 alpha satellite sequence. (1987) (26)
Platelet monoamine oxidase: specific activity and turnover number in headache. (1982) (26)
Localisation of neurone-specific enolase (ENO2) to 12p13. (1990) (26)
Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression. (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)
The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome. (1992) (26)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
Presence of two forms of fumarase (fumarate hydratase E.C. 4.2.1.2) in mammalian cells: Immunological characterization and genetic analysis in somatic cell hybrids. Confirmation of the assignment of a gene necessary for the enzyme expression to human chromosome 1 (1975) (25)
Analysis of the 5' regulatory region of the human Norrie's disease gene: evidence that a non-translated CT dinucleotide repeat in exon one has a role in controlling expression. (1999) (25)
Report of the committee on the genetic constitution of chromosome 12. (1990) (24)
Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb. (2000) (24)
Analysis of proteins synthesized in mitochondria of cultured mammalian cells. An assessment of current approaches and problems in interpretation. (1976) (24)
Localisation of the gene for human aromatic L-amino acid decarboxylase (DDC) to chromosome 7p13-->p11 by in situ hybridisation. (1992) (23)
The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis. (1990) (23)
Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease (2010) (23)
A follow‐up case–control association study of tractable (druggable) genes in recurrent major depression (2011) (23)
Analysis of the 5HT‐2A T102C receptor polymorphism and psychotic symptoms in Alzheimer's disease (2007) (23)
Quantitative trait loci for IQ and other complex traits: single‐nucleotide polymorphism genotyping using pooled DNA and microarrays (2006) (23)
Familiality and SNP heritability of age at onset and episodicity in major depressive disorder (2015) (22)
The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression. (2013) (22)
Long-range physical mapping around the human steroid sulfatase locus. (1990) (22)
Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution. (2014) (22)
Allelic variation at the A218C tryptophan hydroxylase polymorphism influences agitation and aggression in Alzheimer's disease (2004) (22)
Variation in regulation of steroid sulphatase locus in mammals (1983) (22)
ATP-binding cassette sub-family F member 1 (ABCF1) is identified as a putative therapeutic target of escitalopram in the inflammatory cytokine pathway (2013) (21)
Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array (2017) (21)
Copy number variants and therapeutic response to antidepressant medication in major depressive disorder (2014) (21)
High-resolution comparative mapping of the proximal region of the mouse X chromosome. (1995) (21)
Long-range organization of reiterated sequences, including the SSX1 cDNA at the OATL1 cluster in Xp11.23. (1995) (21)
High-throughput single-nucleotide polymorphism genotyping by fluorescent competitive allele-specific polymerase chain reaction (SNiPTag). (2002) (20)
Steroid sulphatase and the conservation of mammalian X chromosomes (1986) (20)
A Model Incorporating Potential Skewed X‐Inactivation in MZ Girls Suggests that X‐Linked QTLs Exist for Several Social Behaviours Including Autism Spectrum Disorder (2008) (20)
Retinal drusen: harbingers of age, safe havens for trouble. (2009) (20)
Elevated Platelet β-Secretase Activity in Mild Cognitive Impairment (2007) (19)
Cloning of mouse mitochondrial DNA in E. coli affects bacterial viability. (1980) (19)
Sequence analysis and transcript identification within 1.5 MB of DNA deleted together with the NDP and MAO genes in atypical Norrie disease patients presenting with a profound phenotype (2001) (19)
Transcriptomics and the mechanisms of antidepressant efficacy (2016) (19)
Dinucleotide repeat polymorphism at the human dopamine β-hydroxylase (DBH) locus (1992) (19)
A dinucleotide repeat polymorphism at the DMD locus. (1991) (18)
No evidence that extended tracts of homozygosity are associated with Alzheimer's disease (2011) (18)
Leber's hereditary optic neuropathy: Implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation (1995) (18)
Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis. (1988) (18)
Age-Related Macular Degeneration-Associated Genes in Alzheimer Disease. (2015) (18)
Pharmacoproteomic investigation into antidepressant response in two mouse inbred strains (2012) (18)
The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction. (1991) (17)
The role of monoamine oxidase A, MAOA, in the aetiology of antisocial behaviour: the importance of gene-environment interactions. (2005) (17)
Physical mapping of genes and sequences at the end of the human X chromosome short arm (1987) (17)
Genome-wide association study of co-occurring anxiety in major depression (2013) (17)
Differences in the mitochondrially synthesized subunits of human and mouse cytochrome c oxidase (1977) (16)
Alpha7 nicotinic acetylcholine receptor gene and reduced risk of Alzheimer's disease. (2008) (16)
Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease (2016) (16)
Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP) (2018) (16)
Association of the serotonin transporter gene, neuroticism and smoking behaviours (2008) (16)
Organization of the human genome (1994) (15)
Probable assignment of the locus determining human red cell acid phosphatase ACP1 to chromosome 2 using somatic cell hybrids (1974) (15)
Psychiatry and the ‘new genetics’: hunting for genes for behaviour and drug response (2005) (14)
Isolation and detailed characterization of human cell lines resistant to D-threo-chloramphenicol. (1976) (14)
The MAO-A genotype does not modulate resting brain metabolism in adults (2008) (14)
Cytoplasmic transfer of a determinant for chloramphenicol resistance between mammalian cell lines (1978) (14)
Engineering in Genomics [variable number tandem repeats as agents of functional regulation in the genome] (2008) (12)
Characterization of the genomic organization of human carcinoembryonic antigen (CEA): comparison with other family members and sequence analysis of 5' controlling region. (1990) (12)
DETECTING MATERNAL CELL CONTAMINATION IN PRENATAL DIAGNOSIS (1989) (12)
Plasma Complement factor H in Alzheimer's Disease. (2015) (12)
Characterization of a YAC containing part or all of the Norrie disease locus. (1992) (12)
Reduced estimated glomerular filtration rate in Alzheimer's disease (2009) (12)
Quantitative Trait Locus Analysis of Candidate Gene Alleles Associated With Attention Deficit Hyperactivity Disorder ( ADHD ) in Five Genes : DRD 4 , DAT 1 , DRD 5 , SNAP-25 , and 5 HT 1 B (2005) (12)
Commentary on “A Role for the X Chromosome in Sex Differences in Variability in General Intelligence?” (Johnson et al., 2009) (2009) (12)
Elevated platelet beta-secretase activity in mild cognitive impairment. (2007) (12)
Report and abstracts of the Second International Workshop on Human Chromosome 12 mapping 1994. New Haven, Connecticut, June 20-22, 1994. (1994) (11)
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11 (1988) (11)
BACE1 Polymorphisms Do Not Influence Platelet Membrane β-secretase Activity or Genetic Susceptibility for Alzheimer’s Disease in the Northern Irish Population (2008) (11)
Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis. (1999) (10)
Differences in the products of mitochondrial protein synthesis in vivo in Human and mouse cells and their potential use as markers for the mitochondrial genome in human--mouse somatic cell hybrids. (1974) (10)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (vol 41, pg 1088, 2009) (2013) (10)
A Pooled Genome-Wide Association Study of Asperger Syndrome (2015) (10)
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp (1989) (10)
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes (2006) (10)
Investigating the Relationship Between FMR1 Allele Length and Cognitive Ability in Children: A Subtle Effect of the Normal Allele Range on the Normal Ability Range? (2006) (10)
Two new mutations in exon 3 of the NDP gene: S73X and S101F associated with severe and less severe ocular phenotype, respectively (1997) (10)
Association analysis of DAOA and DAO in bipolar disorder: results from two independent case-control studies. (2010) (9)
Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease (2014) (9)
Assignment of the coding sequence for carcinoembryonic antigen (CEA) and normal cross‐reacting antigen (NCA) to human chromosome 19 q 13. (1989) (9)
Biosynthesis of proteins involved with photosynthetic activity in enucleated Acetabularia sp. (1970) (9)
Report of the first international workshop on human chromosome 12 mapping. (1992) (9)
A procedure for the analysis of citrate synthase (E.C. 4.1.3.7) in somatic cell hybrids (1973) (9)
MITOCHONDRIAL ENZYMES IN MAN-MOUSE HYBRID CELLS (1974) (9)
Introduction to genetic epidemiology. (2011) (9)
Apolipoprotein ɛ4 and neuropsychological performance in Alzheimer's disease and vascular dementia (2010) (9)
Statins for the treatment of dementia (Review) (2014) (9)
A de novo splice site mutation in CASK causes FG syndrome‐4 and congenital nystagmus (2017) (8)
Single-nucleotide polymorphism genotyping in DNA pools. (2005) (8)
The role of molecular genetics in the postgenomic era. (2003) (8)
The interleukin 1beta gene promoter polymorphism (-511) acts as a risk factor for psychosis in Alzheimer's dementia. (2004) (8)
Human gene mapping 10.5. Oxford Conference (1990). Update to the Tenth International Workshop on Human Gene Mapping. (1990) (8)
oderation of the Effect of Adolescent-Onset Cannabis se on Adult Psychosis by a Functional Polymorphism n the Catechol-O-Methyltransferase Gene: ongitudinal Evidence of a Gene X Environment nteraction (2005) (8)
Mitochondrial and cytoplasmic forms of fumarate hydratase assigned to chromosome 1. (1976) (8)
Introductory guide to the language of molecular genetics. (2005) (8)
Localization of human liver 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB1) within a YAC contig in Xp11.21. (1997) (7)
Methylation and the fragile X (1991) (7)
Molecular cloning and tissue‐specific expression of mouse kidney 6‐phosphofructo‐2‐kinase/fructose‐2,6‐bisphosphatase (1996) (7)
Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146. (1995) (7)
Variation in RTN3 and PPIL2 Genes Does not Influence Platelet Membrane β-Secretase Activity or Susceptibility to Alzheimer’s Disease in the Northern Irish Population (2009) (7)
Special Notice to Contributors (1996) (7)
Death‐associated protein kinase 1 variation and Parkinson’s disease (2011) (7)
Genetic Organization of the Serotonergic System (2010) (7)
Statins for the treatment of Alzheimer's disease and dementia (2009) (7)
Chasing behaviour genes into the next millennium. (2000) (7)
Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS (1991) (7)
Report of the second X Chromosome Workshop Oxford, UK, January 6–7, 1991 (1991) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
Statins for the prevention of dementia (Review) (2009) (6)
Muscular dystrophy ingirls withX;autosome translocations (1986) (6)
A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1. (1994) (6)
Assignment of the genes for human beta-glucuronidase and mitochondrial malate dehydrogenase to the region pter leads to q22 of chromosome 7. (1977) (6)
P3-209: Genetic variation in the alpha 7 nicotinic acetylcholine receptor is associated with delusional symptoms in Alzheimer's disease (2008) (6)
Genetic Polymorphisms in Stress Response (2007) (6)
Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene (1992) (6)
Studies of heterogeneous mitochondrial populations in a mouse cell line: the effects of selection for or against mitochondrial genomes that confer chloramphenicol resistance (1985) (6)
Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus. (1993) (6)
Validation of single nucleotide polymorphism quantification in pooled DNA samples with SNaPIT™ (2002) (6)
Dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase (DBH) locus. (1992) (5)
Rivastigmine for vascular cognitive impairment (Review) (2013) (5)
Assignment of a gene necessary for the expression of mitochondrial glutamic-oxaloacetic transaminase in human-mouse hybrid cells. (1978) (5)
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome (1990) (5)
Caspi Polymorphism in the 5-HTT Gene Influence of Life Stress on Depression : Moderation by a (2015) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Analysis of the Mitochondrial Enzymes Citrate Synthase (EC 4.1.3.7) and Malate Dehydrogenase (EC 1.1.1.37) in Human-Mouse Somatic Cell Hybrids (1974) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Apolipoprotein epsilon4 and neuropsychological performance in Alzheimer's disease and vascular dementia (2010) (5)
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.) (1980) (5)
Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus. (1993) (4)
Platelet monoamine oxidase: specific activity and turnover number in schizophrenics and their families. (1985) (4)
Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis. Problems due to genetic heterogeneity. (1991) (4)
Bipolar disorder susceptibility region on chromosome 3q29 not confirmed in a case–control association study (2011) (4)
Vascular cognitive impairment (2004) (4)
A DIRECT LIGHT EFFECT ON MAINTAINING PHOTOSYNTHETIC ACTIVITY OF NITELLA CHLOROPLASTS (1970) (4)
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene. (1992) (4)
Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays (2010) (4)
Assessing Individual Differences in Genome-Wide Gene Expression in Human Whole Blood: Reliability Over Four Hours and Stability Over 10 Months (2009) (4)
Rapid Publication Expression of the Dopamine Transporter Gene is Regulated by the 3 0 UTR VNTR : Evidence From Brain and Lymphocytes Using Quantitative RT-PCR (2002) (4)
Calendar of Events: 1991 — 1992 (1991) (4)
Erratum to “TNFR-associated factor-2 (TRAF-2) in Alzheimer’s disease” [Culpan et al. (Neurobiol Aging 2009 July;30(7):1052-60)] (2010) (4)
Localisation of the G gamma-, A gamma-, delta- and beta-globin genes on the short arm of human chromosome 11. (1979) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
A bidirectional YAC walk from the Norrie disease (NDP) locus. (1995) (4)
NRG1 gene in recurrent major depression: No association in a large‐scale case–control association study (2009) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Genetic Basis of Chloramphenicol Resistance in Mouse and Human Cell Lines (1982) (3)
Cognitive prosthetics in Alzheimer's disease: A trial of a novel cell phoned- based reminding system (2010) (3)
A preliminary analysis of the segregation of human hydroxyacyl coenzyme A dehydrogenase in human-mouse somatic cell hybrids. (1976) (3)
Genetic association data from GENDEP, a multicentre European study (2006) (3)
Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp) (1996) (3)
The mammalian Y chromosome: molecular search for the sex-determining gene--summary and perspectives. (1987) (3)
ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA (1995) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
IGF2R and cognitive ability (1999) (3)
Influence of coding variability in APP-Aß metabolism genes in sporadic Alzheimer ’ s disease (2016) (3)
The relationship between human monoamine oxidase A and B (1982) (3)
Sex determination: zinc fingers point in the wrong direction. (1990) (3)
Northern Ireland dementia strategy (2010) (3)
Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis. (1996) (3)
Steroid sulphatase levels in XX males, including observations on two affected cousins (1981) (3)
Proteins made in mitochondria of cultured animal cells. (1975) (3)
Genome-Wide Association Study for Alzheimer's Disease Risk in a Large Cohort Of Clinically Characterized And Neuropathologically Verified Subjects (2010) (3)
Human Gene Mapping 10.5: Oxford Conference 1990 Update to the 10th International Workshop, Oxford, September 1990 (1991) (3)
Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27β (DXS255) (1989) (3)
Psychiatric Genetics: Misbehaving monoamine oxidase gene (1994) (3)
Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease (2011) (2)
DNA analysis and recombination in X-linked retinitis pigmentosa (1990) (2)
Genomewide gene expression profiles as a biological basis for non-shared environment: MZ twins discordant for reading ability (2007) (2)
Methylation analysis of a NGF1-A transcription factor binding-site in the promoter region of the human glucocorticoid receptor gene (NR3C1) (2005) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Assignment of a gene for tryptophanyl-transfer ribonucleic acid synthetase (E.C. 6.1.1.2) to human chromosome 14 (1976) (2)
Advances in Migraine Research and Therapy (1982) (2)
Properties of human monoamine oxidases. (1982) (2)
The Genetics of Human Aggressive Behaviour (2010) (2)
A genome-wide allelic association scan of 1847 DNA markers for general cognitive ability: A five-stage design using DNA pooling (2001) (2)
Molecular genetics of the X chromosome and X-linked diseases. (1986) (2)
Galantamine for vascular cognitive impairment. (2006) (2)
P1-042 A cross-sectional study of the behavioural and psychological symptoms of dementia (BPSD) in 435 patients with Alzheimer's disease (2004) (2)
LACK OF AN ASSOCIATION BETWEEN TESTICULAR CANCERS AND LOW STEROID SULPHATASE ACTIVITY IN PERIPHERAL LEUCOCYTES (1985) (2)
Imprinting, Inactivation and the Behavioural Genetics of the X Chromosome (2011) (2)
S.07.04 CYP2D6 genotype predicts antidepressant dose in the GENDEP project (2010) (2)
Prevalence and Clinical Features of Dementia (2010) (2)
CHLOROPLAST DEVELOPMENT IN CHAROPHYCEAE (1971) (2)
Dinucleotide repeat polymorphism in CEA gene. (1991) (2)
Apolipoprotein epsilon 4 and neuropsychological performance in Alzheimer ' s disease and vascular dementia (2010) (1)
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta. (1992) (1)
THE GENETIC BASIS OF NEUROPSYCHIATRIC SYMPTOMS IN PARKINSON'S DISEASE (2011) (1)
Apolipoproteine E4 allele influences aggressive behaviour in alzheimer's disease (2004) (1)
Contents Vol. 55, 1990 (1990) (1)
Elevated platelet beta-secretase acitvity in MCI (2007) (1)
No association of polymorphisms in the chat locus with late-onset Alzheimer's disease (2002) (1)
Pain Managment and Pharmacological Differences in the Elderly Patient (2006) (1)
Gene-brain-behavior relationships: Evidence that aggression is associated with brain MAO A activity in healthy males (2007) (1)
Molecular genetics of blindness. (1994) (1)
A genome wide scan using 400 non-synonymous SNP markers in DNA pools identifies genes associated with language impairment in children (2003) (1)
Instructions for the preparation of gene mapping reports (1995) (1)
Mitochondrial and cytoplasmic forms of fumarate hydratase assigned to chromosome. (1976) (1)
Dinucleotide repeat polymorphism in CEA gene. (1992) (1)
P.1.15 Association of dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case-control study (BACCS) (2008) (1)
The isolation of an antimycin A-resistant human cell line. (1983) (1)
A holistic approach to variation in dopamine genes. (2000) (1)
DNA pools on 10K genechips: Solving the QTL problem of large samples and large numbers of SNPS (2004) (1)
MITOCHONDRIA, AUTOIMMUNITY, AND ONCOGENESIS (1975) (1)
Expression of the dopamine transporter gene is mediated by genotype: Evidence from brain and lymphocytes using quantitative RT-PCR (2002) (1)
Molecular genetics research in sub-Saharan Africa: how can the international community help? (2014) (1)
P.1.a.018 Association analysis of glucocorticoid receptor gene and the muscarinic cholinergic 2 receptor gene in suicidal behaviour (2011) (1)
Human genetics. Methylation and the fragile X. (1991) (1)
Genome-wide association for major depression through age at onset stratificationGenomic analysis of age at onset in depression (2016) (1)
Genetic polymorphisms predict variationiin intelligence and adult prognosis among children with attention-deficit hyperactivity disorder (2005) (1)
P.3.010 CYP2D6 and CYP2C19 genotypes predict antidepressant dose in the GENDEP project (2010) (1)
Pharmacogenetics of antidepressant response: A polygenic approach. Progress in Neuro-Psychopharmacology and (2016) (1)
Linkage disequilibrium mapping of chromosome 22 in schizophrenia using DNA pooling on Chinese and Scottish populations (1998) (0)
Comparison of mouth swab DNA and PEP DNA as a template for genotyping analysis (2002) (0)
A high resolution genome scan made possible with DNA pooling (1999) (0)
X Inactivation as a Source of Behavioural Differences in Monozygotic Female Twins (2004) (0)
Comparison of whole-genome amplification methods using three genotyping platforms (2006) (0)
GENESiS : creating a composi te index of the vulnerabi l i ty to anxiety and depression in a communi ty-based sample of sibl ings (2007) (0)
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β (1992) (0)
Subject Index Vol. 16, 1976 (1976) (0)
University of Birmingham Familiality and SNP heritability of age at onset and episodicity in major depressive disorder (2015) (0)
Response to comment by Stuart Macgregor (2009) (0)
Assignment of a gene for tryptophanyl-transfer ribonucleic acid synthetase to human chromosome 14. (1976) (0)
SHORT COMMUNICATION Localization of Human Monoamine Oxidase-A Gene to Xpl 1.23- 11.4 by in Situ Hybridization: Implications for Norrie Disease (1989) (0)
S.03.02 Gene-environment interaction in depression (2006) (0)
Linkage analysis of chromosome 1 markers in a sibling study of depression and anxiety (GENESIS) (2002) (0)
CYP2D6 and CYP2C19 association data from GENDEP, a multicentre European study (2006) (0)
Final general discussion (2005) (0)
Subject Index Vol. 56, 1991 (1991) (0)
Candidate genes expression profile associated with antidepressants response: differentiating between baseline "predictors" and longitudinal "targets" (2012) (0)
Subject Index Vol. 16, 1976 (1976) (0)
LibGuides: Pangborn Elementary LibGuide: Reference and Research (2015) (0)
An association scan using pooled DNA and 100k SNPS identifies a 'SNP set' for early reading (2006) (0)
GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings (2000) (0)
Overview of HGM10.5 (1990) (0)
Association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with major depressive disorder (2006) (0)
Index by Keyword (1989) (0)
Subject Index Vol. 61, 1992 (1992) (0)
Beetles and Bobartia : feature (2006) (0)
Linkage disequilibrium mapping of chromosome 8, 13 and 22 linkage regions in schizophrenia using DNA pooling on Chinese and Scottish populations (1999) (0)
A genome scan using non-synonymous SNPs in coding regions and general cognitive ability (2002) (0)
A first episode psychosis case-control genetic association study (2006) (0)
Investigation of the relationship between FMR1 allele length and cognitive/behavioural phenotypes (2004) (0)
Title Genomewide association scan of suicidal thoughts andbehaviour in major depression (2011) (0)
QTLs for general cognitive ability in children (1998) (0)
Polymorphisms in the glucocorticoid receptor gene and susceptibility to major affective disorders (2006) (0)
QTLs for general cognitive ability in children: DNA pooling for chromosome 22 (1998) (0)
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (0)
Network-based integrative analysis of lithium response in bipolar disorder using transcriptomic and GWAS data (2022) (0)
Variation in the BDNF gene contributes to alcohol consumption levels in the population (2005) (0)
A genomewide association scan for GE interplay in childhood (2006) (0)
An evaluation of source of DNA for use in DNA pooling (2001) (0)
Title A central resource for accurate allele frequency estimation frompooled DNA genotyped on DNA microarrays (2005) (0)
QTLs for reading disability at 7 years: Genotyping pooled DNA on 100K SNP microarrays (2005) (0)
Explorer Concordant Association of Insulin Degrading Enzyme Gene ( IDE ) Variants with IDE mRNA , A beta , and Alzheimer ' s Disease (2017) (0)
P3-207: Angiotensin-converting enzyme and the risk of late-onset Alzheimer's disease (2008) (0)
LANGUAGE DELAYS AND PHYSICAL AGGRESSION (2003) (0)
Title Page / Table of Contents / Abstracts (1991) (0)
Genetic Variation in BACE1 Interacting Proteins (RTN3 and PPIL2) does not Influence Susceptibility to Alzheimer’s disease in the Northern Irish Population (2009) (0)
Contents, Vol. 56, 1991 (2004) (0)
Pharmacogenomics: Methods and Protocols (2005) (0)
Studies on steroid sulphatase in mice. Abstr. (1983) (0)
Isolation and characterization of a steroid sulfatase cDNA clone : Genomic deletions in patients with X-chromosome-linked ichthyosis ( human X chromosome / Kallmann syndrome / inactivation ) (0)
of clustered in single-voxel morphometry as a rapid automated method for (2020) (0)
INVESTIGATION OF PLATELET MEMBRANE BETA-SECRETASE ACTIVITY AS A POTENTIAL DIAGNOSTIC BIOMARKER FOR ALZHEIMER'S DISEASE (2011) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Letter: Mitochondria, autoimmunity, and oncogenesis. (1975) (0)
Migraine with and without major depression are genetically different disorders (2012) (0)
P2-400: Statins for the prevention of Alzheimer's disease and dementia (2008) (0)
A dinucleotide repeat polymmorphism at the DMD locus (1991) (0)
Correction to Alia-Klein et al. (2009). (2009) (0)
Profound hypoglycaemia and cognitive impairment. (2002) (0)
The Genetics of Athletic Performance DNA Sport (2017) (0)
Concordant association of functional IDE variant with IDE mRNA, Aß, and Alzheimer's disease (2009) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Allelotyping over 10,000 SNPs using DNA pools and microarrays nominates four SNPs associated with mild mental impairment (2005) (0)
HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE (1995) (0)
Meeting of the british society for developmental biology on the mammalian y chromosome molecular search for the sex determining factor oxford england uk march 1987 (1987) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Fine mapping of Alzheimers disease linkage region on chromosome 10 (2002) (0)
T32 Investigation Of Familial Co-Aggregation And Genetic Correlation Of Age At Onset And Episodicity With Personality Dimensions In Major Depressive Disorder (2017) (0)
Differential diagnosis of apathy and depressive symptoms in Alzheimer’s disease (2006) (0)
Investigating psychosis candidate genes in Alzheimer's disease with psychosis using genome-wide association studies (2009) (0)
Replication of chromosome 4 candidate region for alcohol addiction through DNA pooling and individual genotype association studies with the marker D4S2407 in alcoholic and control japanese groups (2000) (0)
Title Estimating the heritability of reporting stressful life eventscaptured by common genetic variants (2013) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
DNA pooling for genomic scanning - Application to an association study (1998) (0)
Neuropsychological assessment of mild cognitive impairment (2010) (0)
Index by Abstract Number (1989) (0)
Eleventh International Chromosome Conference (2004) (0)
A preliminary analysis of the segregation of human hydroxyacyl coenzyme A dehydrogenase in human-mouse somatic cell hybrids. (1976) (0)
Epigenome-wide association study for Parkinson’s Disease: Oral Presentation: postgraduate scholarship award to attend and present this work at the European Society of Human Genetics (2012) (0)
Exploring the role of drug-metabolising enzymes in antidepressant side effects (2015) (0)
P3-244: Insulin degrading enzyme and the risk of late-onset Alzheimer's disease: A large replication study in a European population (2008) (0)
Assessment of Endosulfan EC based on new risk assessment criteria for Endosulfan ULV (2013) (0)
P3-333: A novel reciprocal and biphasic relationship between membrane cholesterol and β-secretase activity in SH-SY5Y cells and human platelets (2008) (0)
Methylation analysis of 485,577 features in a case-control design for neuropsychiatric symptoms in Parkinson’s Disease (2011) (0)
Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders (2013) (0)
No association of polymorphisms in the cholinergic locus with late-onset Alzheimer's disease. (2002) (0)
Polymorphisms in the serotonin transporter, MAOA and COMT genes and susceptibility to unipolar depression (2004) (0)
Beneficial cognitive effects of treating hypertension are not clear (2007) (0)
Divergent associations between MAO A genotype on anterior cingulate metabolism, MAO A levels and cognitive control (2006) (0)
Report of the committee on the genetic constitution of chromosomes 12 and 13. (1988) (0)
Subject Index Vol. 24, 2007 (2007) (0)
Does COMT promoter methylation regulate gene expression (2005) (0)
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
Gene-environment interaction in depression (2006) (0)
The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression (2013) (0)
P4-062 Alleleic variation at the A218C tryptophan hydroxylase polymorphism influences agitation and aggression in Alzheimer's disease (2004) (0)
Rivastigmine for vascular cognitive impairment. (2005) (0)
Association of COMT with neuroticism (2001) (0)
The epigenetic basis of neuropsychiatric symptoms in Parkinson’s disease (2011) (0)
Evaluation of the clinical effectiveness of FDG-PETCT in the diagnosis of early dementia (2012) (0)
Genetic determinants of non-cognitive symptomatology in Alzheimer's disease. (2004) (0)
Generalized Weakness in a 15-Year-Old Male: A Rare Presentation of Thyrotoxic Paralysis with Normokalemia (2016) (0)
P4-124 The PRNP M129V genetic variant is associated with sporadic Alzheimer's disease in Northern Ireland (2004) (0)
Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (2023) (0)
Localisation of quantitative trait loci responsible for the heritability of language impairment using DNA pooling (2002) (0)
Combined whole genome linkage analysis of extraversion (2005) (0)
Age-related macular degeneration genes in Alzheimer’s disease. (2011) (0)
THE SEARCHFORGENES INFLUENCINGBEHAVIOUR (2004) (0)
P3-255 β-secretase activity in human platelets (2006) (0)
Hypoglycaemia and the elderly (2002) (0)
A BamHI polymorphism at the DBH locus. (1990) (0)
Epigenome-Wide Association Study for Parkinson’s Disease (2014) (0)
Contents Vol. 24, 2007 (2007) (0)
COMT in major depression - UK candidate gene association study (2011) (0)
P01-246-3Q29 case-control association study of co-morbid migraine in bipolar affective disorder (2011) (0)
Retinal microvascular evaluation in Alzheimer's disease. (2015) (0)
P.1.024 Depressive disorder moderates the effect of fat mass and obesity-associated gene (FTO) on body mass index (BMI) (2010) (0)
Genome wide association scan of co-morbid anxiety in major depressive disorder (MDD) [Abstract] (2010) (0)
Genomic odyssey. (1994) (0)
P.1.07 Methylenetetrahydrofolate reductase gene and unipolar depression: focus on personality traits (2007) (0)
P.1.10 The depression case control study in the whole genome association era: results and implications for the future (2008) (0)
P.1.a.009 Meta-analysis of CYP2C19 association with efficacy and side effects of citalopram and escitalopram (2017) (0)
Functional promoter VNTR for MAOA: Identification of two novel alleles and analyses of association with neuroticism, depression and anxiety (2000) (0)
Acknowledgement to assessors (2014) (0)
Characterization of White Creek / Trout Creek of otsego County (0)
LibGuides: Pangborn Elementary LibGuide: RAIL Card (2015) (0)
LibGuides: Pangborn Elementary LibGuide: Home (2015) (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)
Whole genome linkage scan for alcohol consumption in a selected sibling sample (2005) (0)
Abstract from the clinical autonomic research society meetingMolecular studies in patients with serum dopamine beta hydroxylase deficiency (1990) (0)
Genetic research on cognitive ability (2002) (0)
Progress in the search for X-linked behavioural QTLS (2004) (0)
Proceedings: Analysis of the mitochondrial enzymes citrate synthase (EC 4.1.3.7) and malate dehydrogenase (EC 1.1.1.37) in human-mouse somatic cell hybrids. (1974) (0)
Serotonin transporter promoter polymorphism: Expression and gene-environment studies in lymphoblast cell lines from a major depression sample (2005) (0)
ANALYSIS OF THE GENE ENCODING AN X-LINKED VOLTAGE-GATED CHLORIDE CHANNEL IN IDIOPATHIC HYPERCALIURIA (1995) (0)
Duplicate: Behavioral genetics in the postgenomic era (2003) (0)
A molecular genetic study of completed suicide in central Slovenia (2006) (0)
Molecular pathway analysis: Serotonergic and noradrenergic candidate genes in unipolar depression (2002) (0)
Elucidating the genes for the susceptibility to depression and anxiety (2005) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Ian W. Craig?

Ian W. Craig is affiliated with the following schools:

Ian W. Craig's Academic­Influence.com Rankings

Ian W. Craig's Degrees

Similar Degrees You Can Earn

Why Is Ian W. Craig Influential?

Ian W. Craig's Published Works

Published Works

What Schools Are Affiliated With Ian W. Craig?

Ian W. Craig's AcademicInfluence.com Rankings