Neil Risch


Ontology type: schema:Person     


Person Info

NAME

Neil

SURNAME

Risch

Publications in SciGraph latest 50 shown

  • 2019-12 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity in NATURE COMMUNICATIONS
  • 2018-12 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci in NATURE COMMUNICATIONS
  • 2018-03 A large electronic-health-record-based genome-wide study of serum lipids in NATURE GENETICS
  • 2017-12 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure in NATURE COMMUNICATIONS
  • 2017-09 Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study in MOLECULAR PSYCHIATRY
  • 2017-01-31 Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer in NATURE COMMUNICATIONS
  • 2017-01 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation in NATURE GENETICS
  • 2016-07 Common coding variants in the HLA-DQB1 region confer susceptibility to age-related macular degeneration in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-05 A brief note on the resemblance between relatives in the presence of population stratification in HEREDITY
  • 2011-01 Common variants in P2RY11 are associated with narcolepsy in NATURE GENETICS
  • 2009-12 Characterizing the admixed African ancestry of African Americans in GENOME BIOLOGY
  • 2009-11 Ancestry-related assortative mating in Latino populations in GENOME BIOLOGY
  • 2008-12 Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD in BMC MEDICAL GENETICS
  • 2008-10 Genome-wide distribution of ancestry in Mexican Americans in HUMAN GENETICS
  • 2008-06 Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region in HUMAN GENETICS
  • 2008-05 Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease in HUMAN GENETICS
  • 2007-11-22 A genome-wide scan in forty large pedigrees with multiple sclerosis in JOURNAL OF HUMAN GENETICS
  • 2006-07 Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans in HUMAN GENETICS
  • 2006-01 Population stratification confounds genetic association studies among Latinos in HUMAN GENETICS
  • 2005-02 Admixture mapping for hypertension loci with genome-scan markers in NATURE GENETICS
  • 2004-11 Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups in NATURE GENETICS
  • 2004-07 TCR β polymorphisms and multiple sclerosis in GENES & IMMUNITY
  • 2003-10 Immunology: Hepatitis A virus link to atopic disease in NATURE
  • 2003-10 Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome in NATURE GENETICS
  • 2003-03 Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease in NATURE GENETICS
  • 2002-06 Categorization of humans in biomedical research: genes, race and disease in GENOME BIOLOGY
  • 2002-05 Candidate-gene approaches for studying complex genetic traits: practical considerations in NATURE REVIEWS GENETICS
  • 2001-10 Birth Order Effects on Nonverbal IQ Scores in Autism Multiplex Families in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2001-07 Genetic susceptibility to MS: a second stage analysis in Canadian MS families in NEUROGENETICS
  • 2001-04 Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes in NATURE GENETICS
  • 2000-06 Searching for genetic determinants in the new millennium in NATURE
  • 1999-06 Exclusion of Linkage to the HLA Region in Ninety Multiplex Sibships with Autism in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 1999-04 Linkage Disequilibrium Analysis of the Gaucher Disease N370S Mutation in PEDIATRIC RESEARCH
  • 1998-07 A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus in NATURE GENETICS
  • 1997-12 Haemochromatosis HFE and genetic complexity in NATURE GENETICS
  • 1997-09 The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein in NATURE GENETICS
  • 1995-11 Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib–pair linkage analysis in NATURE GENETICS
  • 1995-09 A genetic basis for familial aggregation in multiple sclerosis in NATURE
  • 1995-09 Reply to “ITD in Ashkenazi Jews — genetic drift or selection?” in NATURE GENETICS
  • 1995-06 Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7 in NATURE GENETICS
  • 1995-05 Localization of a gene for partial epilepsy to chromosome 10q in NATURE GENETICS
  • 1995-02 Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population in NATURE GENETICS
  • 1994-06 Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease in NATURE GENETICS
  • 1993-12 Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q in NATURE GENETICS
  • 1993-11 Linkage studies of psychiatric disorders in EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
  • 1993-01 Diminished support for linkage between manic depressive illness and X–chromosome markers in three Israeli pedigrees in NATURE GENETICS
  • 1993-01 The calculation of breast cancer risk for women with a first degree family history of ovarian cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 1987-03 Genetic linkage between X-chromosome markers and bipolar affective illness in NATURE
  • 1985-07 Segregation analysis of human hand preference in BEHAVIOR GENETICS
  • 1983-09 Estimating morbidity risks in relatives: The effect of reduced fertility in BEHAVIOR GENETICS
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