Christopher D Brown
University of Pennsylvania
H-index: 54
North America-United States
Top articles of Christopher D Brown
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits | Cell metabolism | Maria C Costanzo Marcin von Grotthuss Jeffrey Massung Dongkeun Jang Lizz Caulkins | 2023/4/4 |
The genetic and evolutionary basis of gene expression variation in East Africans | Genome Biology | Derek E Kelly Shweta Ramdas Rong Ma Renata A Rawlings-Goss Gregory R Grant | 2023/2/24 |
Uncovering Active Bacterial Symbionts in Three Species of Pollen-feeding Beetles (Nitidulidae: Meligethinae) | Microbial ecology | Emiliano Mancini Simone Sabatelli Yi Hu Sara Frasca Andrea Di Giulio | 2023/1 |
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts | Communications biology | Chaojie Yang Jenna Veenstra Traci M Bartz Matthew C Pahl Brian Hallmark | 2023/8/16 |
Evaluating the Contribution of Cell Type–Specific Alternative Splicing to Variation in Lipid Levels | Circulation: Genomic and Precision Medicine | Katerina AB Gawronski William P Bone YoSon Park Evanthia E Pashos Brandon M Wenz | 2023/6 |
The power of genetic diversity in genome-wide association studies of lipids (vol 600, pg 675, 2021) | Nature | Sarah E Graham Shoa L Clarke Kuan-Han H Wu Stavroula Kanoni Greg JM Zajac | 2023/5/26 |
Self-expanding transcatheter vs surgical aortic valve replacement in intermediate-risk patients: 5-year outcomes of the SURTAVI randomized clinical trial | JAMA cardiology | Nicolas M Van Mieghem G Michael Deeb Lars Søndergaard Eberhard Grube Stephan Windecker | 2022/10/1 |
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation | Nature genetics | Marijana Vujkovic Shweta Ramdas Kim M Lorenz Xiuqing Guo Rebecca Darlay | 2022/6 |
Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets | Alzheimer's & dementia | Karen Nuytemans Marina Lipkin Vasquez Liyong Wang Derek Van Booven Antony J Griswold | 2022/10 |
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids | The American Journal of Human Genetics | Shweta Ramdas Jonathan Judd Sarah E Graham Stavroula Kanoni Yuxuan Wang | 2022/8/4 |
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease | Nature genetics | Hongbo Liu Tomohito Doke Dong Guo Xin Sheng Ziyuan Ma | 2022/7 |
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis | Genome biology | Stavroula Kanoni Sarah E Graham Yuxuan Wang Ida Surakka Shweta Ramdas | 2022/12/27 |
The impact of surgical delay on resectability of colorectal cancer: An international prospective cohort study | Colorectal Disease | COVIDSurg Collaborative | 2022/6 |
Outcomes of gynecologic cancer surgery during the COVID-19 pandemic: an international, multicenter, prospective CovidSurg-Gynecologic Oncology Cancer study | American Journal of Obstetrics & Gynecology | Christina Fotopoulou Tabassum Khan Juraj Bracinik James Glasbey Nadeem Abu-Rustum | 2022/11/1 |
Transcriptome-wide association analysis identifies DACH1 as a kidney disease risk gene that contributes to fibrosis | medRxiv | Dorothy M Chen Ruocheng Dong Linda Kachuri Thomas Hoffmann Yu Jiang | 2023/5/5 |
Functional characterization of organoids derived from irreversibly damaged liver of patients with NASH | Hepatology | Sarah McCarron Brooke Bathon Donna M Conlon Deepti Abbey Daniel J Rader | 2021/10 |
Ancestry‐specific intronic variants on the APOEɛ4 haplotype influence enhancer activity and interaction with APOE promoter | Alzheimer's & dementia | Karen Nuytemans Marina Lipkin Vasquez Farid Rajabli Katrina Celis Oded Oron | 2021/12 |
Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments | Nature genetics | Xin Sheng Yuting Guan Ziyuan Ma Junnan Wu Hongbo Liu | 2021/9 |
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease | Cell | Olivia M de Goede Daniel C Nachun Nicole M Ferraro Michael J Gloudemans Abhiram S Rao | 2021/5/13 |
Variant‐to‐gene mapping in human microglial cell models with CRISPR validation implicates RTFDC1 at the Alzheimer’s disease ‘CASS4’ locus | Alzheimer's & Dementia | Elizabeth Burton Mariana Argenziano Kieona Cook Sumei Lu Elisabetta Manduchi | 2021/12 |
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