R. L. Chisholm

发表

Generalization of Variants Identified by Genome‐Wide Association Studies for Electrocardiographic Traits in African Americans

Melissa A. Basford, Janina M. Jeff, Wendy A. Wolf, 2013, Annals of human genetics.

High Density GWAS for LDL Cholesterol in African Americans Using Electronic Medical Records Reveals a Strong Protective Variant in APOE

William K. Thompson, C. Carlson, T. Manolio, 2012, Clinical and translational science.

Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries

Iman A. Mohammed, M. Peluso, S. Chanock, 2022, Nature Genetics.

Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans.

T. Manolio, D. Roden, J. Denny, 2017, Journal of the American College of Cardiology.

Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects

Marylyn D. Ritchie, Joshua C. Denny, Teri E. Klein, 2018, Clinical pharmacology and therapeutics.

Prepublication data sharing

Christopher P Austin, Rolf Apweiler, Tatsuhiko Tsunoda, 2009, Nature.

Characterizing genetic variants for clinical action

Kensaku Kawamoto, Nazneen Rahman, Elaine Lyon, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

Genomic medicine year in review: 2021.

Marc S. Williams, C. Bult, M. Relling, 2021, American journal of human genetics.

Towards BioDBcore: a community-defined information specification for biological databases

Chris F. Taylor, John M. Hancock, Charles E. Cook, 2011, Database : the journal of biological databases and curation.

Returning integrated genomic risk and clinical recommendations: the eMERGE study.

Melissa L. Habrat, Jorge A. Alsip, Kathleen F. Mittendorf, 2023, Genetics in medicine : official journal of the American College of Medical Genetics.

Intravenous gamma globulin in the management of patients with hypogammaglobulinemia.

R. Petty, J. Cassidy, K. Mccall, 1978, The Journal of allergy and clinical immunology.

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.

Melissa A. Basford, C. Chute, T. Manolio, 2011, American journal of human genetics.

Gene Ontology Consortium: The Gene Ontology (GO) database and informatics resource

B Marshall, Eurie L. Hong, Chandra L. Theesfeld, 2004, Nucleic Acids Res..

Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network

Melissa A. Basford, John J. Connolly, Terrie E. Kitchner, 2016, Clinical pharmacology and therapeutics.

Pathogenesis of abdominal aortic aneurysms: a multidisciplinary research program supported by the National Heart, Lung, and Blood Institute.

J D Humphrey, H Kuivaniemi, J. Humphrey, 2001, Journal of vascular surgery.

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study

Suzette J. Bielinski, Christopher G. Chute, Joshua C. Denny, 2012, J. Am. Medical Informatics Assoc..

A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough

J G Linneman, William K. Thompson, Pedro L. Teixeira, 2015, The Pharmacogenomics Journal.

Assessing the understanding of biobank participants

Wendy A. Wolf, K. Ormond, R. Chisholm, 2009, American journal of medical genetics. Part A.

Towards BioDBcore: a community-defined information specification for biological databases

Tin Wee Tan, Chris F. Taylor, Carole A. Goble, 2010, Database J. Biol. Databases Curation.

Admixture Mapping and Subsequent Fine-Mapping Suggests a Biologically Relevant and Novel Association on Chromosome 11 for Type 2 Diabetes in African Americans

Melissa A. Basford, Janina M. Jeff, Wendy A. Wolf, 2014, PloS one.

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

Frequency of genomic incidental findings among 21,915 eMERGE network participants

Magalie S Leduc, Marc S. Williams, N. Lennon, 2020, Genetics in Medicine.

Assessing the understanding of biobank participants

Wendy A. Wolf, K. Ormond, I. Helenowski, 2009, American journal of medical genetics. Part A.

Northwestern University Initiatives on Resource and Education Development for Collaborative AI in Learning Health System

David M. Liebovitz, Marianne M Green, M. Markl, 2022 .

The two alpha-tubulin genes of Chlamydomonas reinhardi code for slightly different proteins

R. Chisholm, C. Silflow, L. Ranum, 1985, Molecular and cellular biology.

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

Melissa A. Basford, John J. Connolly, Marc S. Williams, 2013, Genetics in Medicine.

Northwestern University resource and education development initiatives to advance collaborative artificial intelligence across the learning health system

R. Wunderink, K. Michelson, J. Starren, 2024, Learning health systems.

Deciphering the impact of genomic variation on function.

William H. Majoros, Neva C. Durand, Alan F. Rubin, 2024, Nature.

Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm

William K. Thompson, Yoonjung Yoonie Joo, P. Peissig, 2023, PloS one.

Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

Benjamin J. Polacco, Robyn M. Kaake, Steven J. Schrodi, 2023, Nature communications.