检索结果 - Anshika Srivastava
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Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations 由 Anshika Srivastava, Rudra Kumar Pandey, Prajjval Pratap Singh, Pramod Kumar, Avinash Arvind Rasalkar, Rakesh Tamang, George van Driem, Pankaj Shrivastava, Gyaneshwer Chaubey
出版 2020Artigo -
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<i>De novo</i>dominant<i>ASXL3</i>mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome 由 Anshika Srivastava, K.C. Ritesh, Yao-Chang Tsan, Rosy Liao, Fengyun Su, Xuhong Cao, Mark C. Hannibal, Catherine E. Keegan, Arul M. Chinnaiyan, Donna M. Martin, Stephanie Bielas
出版 2015Artigo -
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Genetic analysis of CHARGE syndrome identifies overlapping molecular biology 由 Amanda Moccia, Anshika Srivastava, Jennifer Skidmore, John Bernat, Marsha M. Wheeler, Jessica X. Chong, Deborah A. Nickerson, Michael J. Bamshad, Margaret A. Hefner, Donna M. Martin, Stephanie Bielas
出版 2018Artigo -
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Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India 由 Anshika Srivastava, Audditiya Bandopadhyay, Debashruti Das, Rudra Kumar Pandey, Vanya Singh, Nargis Khanam, Nikhil Srivastava, Prajjval Pratap Singh, Pavan Kumar Dubey, Abhishek Pathak, Pranav Gupta, Niraj Rai, Gazi Nurun Nahar Sultana, Gyaneshwer Chaubey
出版 2020Artigo -
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Photosensitivity and type I IFN responses in cutaneous lupus are driven by epidermal-derived interferon kappa 由 Mrinal K. Sarkar, Grace A. Hile, Lam C. Tsoi, Xianying Xing, Jianhua Liu, Yun Liang, Céline C. Berthier, William R. Swindell, Matthew T. Patrick, Shuai Shao, Pei‐Suen Tsou, Ranjitha Uppala, Maria A. Beamer, Anshika Srivastava, Stephanie Bielas, Paul W. Harms, Spiro Getsios, James T. Elder, John J. Voorhees, Jóhann E. Guðjónsson, J. Michelle Kahlenberg
出版 2018Artigo -
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Genotype-phenotype correlations in individuals with pathogenic<i>RERE</i>variants 由 Valerie K. Jordan, Brieana Fregeau, Xiaoyan Ge, Jessica L. Giordano, Ronald J. Wapner, Tuğçe B. Balcı, Jennefer N. Carter, John Bernat, Amanda Moccia, Anshika Srivastava, Donna M. Martin, Stephanie Bielas, John Pappas, Melissa Svoboda, Marlène Rio, Nathalie Boddaert, Vincent Cantagrel, Andrea M. Lewis, Fernando Scaglia, Jennefer N. Kohler, Jonathan A. Bernstein, Annika M. Dries, Jill A. Rosenfeld, Colette DeFilippo, Willa Thorson, Yaping Yang, Elliott H. Sherr, Weimin Bi, Daryl A. Scott
出版 2018Artigo -
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Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations 由 Elizabeth A. Werren, Emily Peirent, Henna Jäntti, Alba Guxholli, Kinshuk Raj Srivastava, Naama Orenstein, Vinodh Narayanan, Wojciech Wiszniewski, Mateusz Dawidziuk, Paweł Gawliński, Muhammad Umair, Amjad Khan, Shahid Niaz Khan, David Geneviève, Daphné Lehalle, Koen L.I. van Gassen, Jacques C. Giltay, Renske Oegema, Richard H. van Jaarsveld, Rafiullah Rafiullah, Gudrun Rappold, Rachel Rabin, John Pappas, Marsha M. Wheeler, Michael J. Bamshad, Yao-Chang Tsan, Matthew B. Johnson, Catherine E. Keegan, Anshika Srivastava, Stephanie Bielas
出版 2024Artigo
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