Neil Risch

发表

The calculation of breast cancer risk for women with a first degree family history of ovarian cancer

N. Risch, W. Thompson, E. Claus, 1993, Breast Cancer Research and Treatment.

Human gene for torsion dystonia located on chromosome 9q32-q34

Stanley Fahn, Robert E. Burke, Patricia L. Kramer, 1989, Neuron.

Narcolepsy is strongly associated with the T-cell receptor alpha locus (vol 41, pg 708, 2009)

Christian Gieger, Thomas Meitinger, Emmanuel Mignot, 2014 .

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

Christine Klein, Geetha Senthil, Michele Tagliati, 2006, The New England journal of medicine.

A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program.

Eric Boerwinkle, Stephen T Turner, Steven C Hunt, 2003, American journal of hypertension.

Positional Cloning of the Human Quantitative Trait Locus Underlying Taste Sensitivity to Phenylthiocarbamide

Mark Leppert, Dennis Drayna, Hilary Coon, 2003, Science.

Admixture mapping and the role of population structure for localizing disease genes.

Xiaofeng Zhu, Hua Tang, N. Risch, 2008, Advances in genetics.

Human genetic variation recognizes functional elements in noncoding sequence.

David Lomelin, Eric Jorgenson, N. Risch, 2010, Genome research.

Automated Assay of Telomere Length Measurement and Informatics for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort

Pui-Yan Kwok, Carlos Iribarren, Dana Ludwig, 2015, Genetics.

Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array.

Simon Cawley, Earl Hubbell, Pui-Yan Kwok, 2011, Genomics.

The SNP Endgame: A Multidisciplinary Approach *

N. Risch, Neil Risch, 2005 .

Validation of Electronic Health Records for the Assessment of Statin Dosing In Research

Carlos Iribarren, Ronald M. Krauss, Akinyemi Oni-Orisan, 2017 .

Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm.

Pui-Yan Kwok, Jeremy Gollub, Carlos Iribarren, 2011, Genomics.

A brief history of human disease genetics

Mark I. McCarthy, Heidi L. Rehm, Jay Shendure, 2020, Nature.

Categorization of humans in biomedical research: genes, race and disease

Hua Tang, Elad Ziv, N. Risch, 2002, Genome Biology.

The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change

Tanushree Haldar, Carlos Iribarren, Ronald M. Krauss, 2020, npj Genomic Medicine.

Estimating kinship in admixed populations.

Hua Tang, Thomas J Hoffmann, Timothy Thornton, 2012, American journal of human genetics.

Homozygosity and linkage disequilibrium.

Chiara Sabatti, C. Sabatti, N. Risch, 2002, Genetics.

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease

Margaret A. Pericak-Vance, Jonathan L. Haines, Bradley T. Hyman, 1997 .

Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer

Pui-Yan Kwok, Olle Melander, Tobias Nordström, 2017, Nature Communications.

Common variants in P2RY11 are associated with narcolepsy

Christian Gieger, Poul Jennum, Thomas Meitinger, 2010, Nature Genetics.

A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.

Pui-Yan Kwok, Daniel J Schaid, John S Witte, 2015, Cancer discovery.

Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups

N. Risch, J. Mountain, Neil Risch, 2004, Nature Genetics.

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

Xiaofeng Zhu, Tamar Sofer, Joshua C Denny, 2017, PLoS genetics.

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes

N. Freimer, N. Risch, K. Giacomini, 2001, Nature Genetics.

Global transcriptional response to interferon is a determinant of HCV treatment outcome and is modified by race

Robert Tibshirani, Aijaz Ahmed, Garry P Nolan, 2006, Hepatology.

Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological research.

Rui Mei, Hui-Ju Tsai, Elad Ziv, 2005, American journal of public health.

Genetic variation in aldosterone synthase predicts plasma glucose levels

David Botstein, Richard A. Olshen, Low-Tone Ho, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP).

Steven C. Hunt, Eric Boerwinkle, Nicholas J. Schork, 2002, Hypertension.

A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci

Thomas J Hoffmann, Mark N Kvale, Eric Jorgenson, 2018, Genetics.

Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib–pair linkage analysis

Margot Albus, Richard P. Ebstein, Wolfgang Maier, 1995, Nature Genetics.

Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.

Jun Li, Richard M Myers, Themistocles L Assimes, 2008, Human molecular genetics.