Pages that link to "Q7027511"
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The following pages link to Nick Martin (Q7027511):
Displayed 50 items.
- Lindon Eaves (Q6552596) (← links)
- Twin Research and Human Genetics (Q7858271) (← links)
- Familial resemblance of borderline personality disorder features: genetic or cultural transmission? (Q21090066) (← links)
- Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo (Q21092433) (← links)
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases (Q21144915) (← links)
- Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer (Q21144952) (← links)
- Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness (Q21144980) (← links)
- Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings (Q21145269) (← links)
- A genome-wide association study identifies five loci influencing facial morphology in Europeans (Q21563366) (← links)
- Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata (Q21710707) (← links)
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence (Q22337141) (← links)
- Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language (Q22337331) (← links)
- Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group (Q23747515) (← links)
- GWAS of 126,559 individuals identifies genetic variants associated with educational attainment (Q24289119) (← links)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (Q24289484) (← links)
- Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults (Q24301468) (← links)
- Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. (Q24533776) (← links)
- POT1 loss-of-function variants predispose to familial melanoma (Q24563091) (← links)
- Evidence for an interaction between age at first drink and genetic influences on DSM-IV alcohol dependence symptoms (Q24595696) (← links)
- Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis (Q24596087) (← links)
- Genome-wide association meta-analysis identifies new endometriosis risk loci (Q24597781) (← links)
- Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample (Q24598131) (← links)
- Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis (Q24601618) (← links)
- Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. (Q24612743) (← links)
- Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma (Q24619042) (← links)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (Q24620065) (← links)
- Biological, clinical and population relevance of 95 loci for blood lipids (Q24622541) (← links)
- Genome-wide association studies identify four ER negative-specific breast cancer risk loci (Q24622610) (← links)
- A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality (Q24625579) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder (Q24634497) (← links)
- Genetic influences on handedness: data from 25,732 Australian and Dutch twin families (Q24642845) (← links)
- A high-density association screen of 155 ion transport genes for involvement with common migraine (Q24653482) (← links)
- Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis (Q24656053) (← links)
- A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color (Q24656429) (← links)
- Common variants in the trichohyalin gene are associated with straight hair in Europeans (Q24657996) (← links)
- A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation (Q24680346) (← links)
- Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan (Q24816052) (← links)
- A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip (Q26995717) (← links)
- Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels (Q27324181) (← links)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association (Q27653381) (← links)
- The subtlety of sex-atypicality (Q28139072) (← links)
- Genome-wide association study reveals two new risk loci for bipolar disorder (Q28235753) (← links)
- Genetic epidemiology of alcohol-induced blackouts (Q28247723) (← links)
- Heritability of borderline personality disorder features is similar across three countries (Q28256538) (← links)
- Novel variants in growth differentiation factor 9 in mothers of dizygotic twins (Q28262009) (← links)
- Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation (Q28264333) (← links)
- Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (Q28267893) (← links)
- Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium (Q28274406) (← links)