Ian W. Craig
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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
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(Suggest an Edit or Addition)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)
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- 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)
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- 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)
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- 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)
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- 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)
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What Schools Are Affiliated With Ian W. Craig?
Ian W. Craig is affiliated with the following schools: