sameAs
P185
Familial resemblance of borderline personality disorder features: genetic or cultural transmission?Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivoSix novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesMultiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancerCommon genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessAssumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblingsA genome-wide association study identifies five loci influencing facial morphology in EuropeansGenome-wide linkage and association analyses implicate FASN in predisposition to Uterine LeiomyomataThe ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligenceRecently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or languageGWAS of 126,559 individuals identifies genetic variants associated with educational attainmentThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataCommon Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adultsGenomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.POT1 loss-of-function variants predispose to familial melanomaEvidence for an interaction between age at first drink and genetic influences on DSM-IV alcohol dependence symptomsMeta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitisGenome-wide association meta-analysis identifies new endometriosis risk lociDyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sampleGenome-wide association study identifies a locus at 7p15.2 associated with endometriosisMeta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanomaGenome-wide association analyses identify 18 new loci associated with serum urate concentrationsBiological, clinical and population relevance of 95 loci for blood lipidsGenome-wide association studies identify four ER negative-specific breast cancer risk lociA genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personalityHundreds of variants clustered in genomic loci and biological pathways affect human heightGenome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderGenetic influences on handedness: data from 25,732 Australian and Dutch twin familiesA high-density association screen of 155 ion transport genes for involvement with common migraineAssociations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysisA single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colorCommon variants in the trichohyalin gene are associated with straight hair in EuropeansA three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variationEvaluation of multiple displacement amplification in a 5 cM STR genome-wide scan.A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hipNovel genetic loci underlying human intracranial volume identified through genome-wide associationGenome-wide association study reveals two new risk loci for bipolar disorderGenetic epidemiology of alcohol-induced blackoutsHeritability of borderline personality disorder features is similar across three countries
P50
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P50
description
Australian human behavior geneticist
@en
australischer Genetiker
@de
genetista australiano
@es
klinische genetica uit Australië
@nl
xenetista australianu
@ast
عالم وراثة أسترالي
@ar
name
Nick Martin (scientist)
@nl
Nick Martin
@ast
Nick Martin
@ca
Nick Martin
@de
Nick Martin
@en
Nick Martin
@es
Nick Martin
@fr
Nick Martin
@ga
Nick Martin
@sl
Nick Martin
@sq
type
label
Nick Martin (scientist)
@nl
Nick Martin
@ast
Nick Martin
@ca
Nick Martin
@de
Nick Martin
@en
Nick Martin
@es
Nick Martin
@fr
Nick Martin
@ga
Nick Martin
@sl
Nick Martin
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altLabel
Martin NG
@en
N G Martin
@en
Nicholas G Martin
@en
Nicholas G Martin
@nl
Nicholas G. Martin
@en
Nicholas Gordon Martin
@en
Nicholas Martin
@en
prefLabel
Nick Martin (scientist)
@nl
Nick Martin
@ast
Nick Martin
@ca
Nick Martin
@de
Nick Martin
@en
Nick Martin
@es
Nick Martin
@fr
Nick Martin
@ga
Nick Martin
@sl
Nick Martin
@sq
P1006
P214
P244
P1006
P1153
35376988300
P166
P184
P19
P21
P214
P244
P2456
P27
P31
P496
0000-0003-4069-8020
P569
1950-02-14T00:00:00Z
P734
P737
P7859
lccn-n88146147