Another Round of “Clue” to Uncover the Mystery of Complex Traits

por Verma, Shefali Setia, Ritchie, Marylyn D.
Publicado 2018

Leveraging electronic health record data for endometriosis research

por Penrod, Nadia, Okeh, Chelsea, Velez Edwards, Digna R., Barnhart, Kurt, Senapati, Suneeta, Verma, Shefali S.
Publicado 2023

What about the environment? Leveraging multi-omic datasets to characterize the environment’s role in human health

por Passero, Kristin, Setia-Verma, Shefali, McAllister, Kimberly, Manrai, Arjun, Patel, Chirag, Hall, Molly
Publicado 2021

Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression()

por Li, Binglan, Verma, Shefali S., Veturi, Yogasudha C., Verma, Anurag, Bradford, Yuki, Haas, David W., Ritchie, Marylyn D.
Publicado 2018

A simulation study investigating power estimates in phenome-wide association studies

por Verma, Anurag, Bradford, Yuki, Dudek, Scott, Lucas, Anastasia M., Verma, Shefali S., Pendergrass, Sarah A., Ritchie, Marylyn D.
Publicado 2018

16 Cross-ancestry analysis of preeclampsia identifies novel maternal susceptibility loci

por Greene, Catherine A., Jasper, Elizabeth A., Hellwege, Jacklyn, Verma, Shefali S., Xiao, Brenda, Edwards, Todd, Velez Edwards, Digna R.
Publicado 2023

Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits

por Choe, Eun Kyung, Shivakumar, Manu, Verma, Anurag, Verma, Shefali Setia, Choi, Seung Ho, Kim, Joo Sung, Kim, Dokyoon
Publicado 2022

Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies

por Li, Binglan, Veturi, Yogasudha, Bradford, Yuki, Verma, Shefali S., Verma, Anurag, Lucas, Anastasia M., Haas, David W., Ritchie, Marylyn D.
Publicado 2019

Genome-Wide Association Study of Breast Density among Women of African Ancestry

por Verma, Shefali Setia, Guare, Lindsay, Ehsan, Sarah, Gastounioti, Aimilia, Scales, Gabrielle, Ritchie, Marylyn D., Kontos, Despina, McCarthy, Anne Marie
Publicado 2023

Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202

por Verma, Anurag, Bradford, Yuki, Verma, Shefali S., Pendergrass, Sarah A., Daar, Eric S., Venuto, Charles, Morse, Gene D., Ritchie, Marylyn D., Haas, David W.
Publicado 2017

Collective feature selection to identify crucial epistatic variants

por Verma, Shefali S., Lucas, Anastasia, Zhang, Xinyuan, Veturi, Yogasudha, Dudek, Scott, Li, Binglan, Li, Ruowang, Urbanowicz, Ryan, Moore, Jason H., Kim, Dokyoon, Ritchie, Marylyn D.
Publicado 2018

Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population

por Verma, Shefali S., Keat, Karl, Li, Binglan, Hoffecker, Glenda, Risman, Marjorie, Sangkuhl, Katrin, Whirl-Carrillo, Michelle, Dudek, Scott, Verma, Anurag, Klein, Teri E., Ritchie, Marylyn D., Tuteja, Sony
Publicado 2022

Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols

por Moore, Carrie B., Verma, Anurag, Pendergrass, Sarah, Verma, Shefali S., Johnson, Daniel H., Daar, Eric S., Gulick, Roy M., Haubrich, Richard, Robbins, Gregory K., Ritchie, Marylyn D., Haas, David W.
Publicado 2014

Rare variants in drug target genes contributing to complex diseases, phenome-wide

por Verma, Shefali Setia, Josyula, Navya, Verma, Anurag, Zhang, Xinyuan, Veturi, Yogasudha, Dewey, Frederick E., Hartzel, Dustin N., Lavage, Daniel R., Leader, Joe, Ritchie, Marylyn D., Pendergrass, Sarah A.
Publicado 2018

Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

por Verma, Shefali Setia, Josyula, Navya, Verma, Anurag, Zhang, Xinyuan, Veturi, Yogasudha, Dewey, Frederick E., Hartzel, Dustin N., Lavage, Daniel R., Leader, Joe, Ritchie, Marylyn D., Pendergrass, Sarah A.
Publicado 2018

An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer

por Oh, Jong Jin, Shivakumar, Manu, Miller, Jason, Verma, Shefali, Lee, Hakmin, Hong, Sung Kyu, Lee, Sang Eun, Lee, Younghee, Lee, Soo Ji, Sung, Joohon, Kim, Dokyoon, Byun, Seok-Soo
Publicado 2019

Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer

por Oh, Jong Jin, Shivakumar, Manu, Miller, Jason, Verma, Shefali, Lee, Hakmin, Hong, Sung Kyu, Lee, Sang Eun, Lee, Younghee, Lee, Soo Ji, Sung, Joohon, Kim, Dokyoon, Byun, Seok-Soo
Publicado 2020

Genetics of height and risk of atrial fibrillation: A Mendelian randomization study

por Levin, Michael G., Judy, Renae, Gill, Dipender, Vujkovic, Marijana, Verma, Shefali S., Bradford, Yuki, Ritchie, Marylyn D., Hyman, Matthew C., Nazarian, Saman, Rader, Daniel J., Voight, Benjamin F., Damrauer, Scott M.
Publicado 2020

Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions

por Xiao, Brenda, Velez Edwards, Digna R., Lucas, Anastasia, Drivas, Theodore, Gray, Kathryn, Keating, Brendan, Weng, Chunhua, Jarvik, Gail P., Hakonarson, Hakon, Kottyan, Leah, Elhadad, Noemie, Wei, Wei‐Qi, Luo, Yuan, Kim, Dokyoon, Ritchie, Marylyn, Verma, Shefali Setia
Publicado 2023

Post-induction Measurable Residual Disease Using Multicolor Flow Cytometry Is Strongly Predictive of Inferior Clinical Outcome in the Real-Life Management of Childhood T-Cell Acute...

por Tembhare, Prashant R., Narula, Gaurav, Khanka, Twinkle, Ghogale, Sitaram, Chatterjee, Gaurav, Patkar, Nikhil V., Prasad, Maya, Badrinath, Yajamanam, Deshpande, Nilesh, Gudapati, Pratyusha, Verma, Shefali, Sanyal, Mahima, Kunjachan, Florence, Mangang, Gunit, Gujral, Sumeet, Banavali, Shripad, Subramanian, Papagudi G.
Publicado 2020