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职业迁徙
个人简介
Her clinical research interests include creatine deficiency disorders, pyridoxine dependent epilepsy, inherited neurotransmitter disorders. She provides genetic diagnostics for epilepsy and pediatric movement disorders.
Dr. Andrews and her team characterized first knock-out aldh7a1 zebrafish to study neuropathogenesis of pyridoxine dependent epilepsy.
Dr. Andrews and her team characterized first knock-out aldh7a1 zebrafish to study neuropathogenesis of pyridoxine dependent epilepsy.
研究兴趣
论文共 73 篇作者统计合作学者相似作者
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Jennifer Goldstein, Amanda Thomas-Wilson,Emily Groopman,Vimla Aggarwal,Simona Bianconi, Raquel Fernandez, Kim Hart,Nicola Longo, Nicole Liang, Daniel Reich, Heidi Wallis, Meredith Weaver,
Molecular Genetics and Metabolismno. 1 (2024): 108362-108362
Genetics in Medicine Open (2024): 101186
Hui-Min Lee,Saadet Mercimek-Andrews,Gabriella Horvath, Diana Marchese, Richard E. Poulin III, Alexis Krolick, Kati-Lyn Tierney, Jasmine Turna, Judy Wei,Wuh-Liang Hwu
Orphanet Journal of Rare Diseasesno. 1 (2024): 1-16
Nihal Almenabawy,Shalini Bahl, Alyssa-Lyn Ostlund, Shailly Ghai-Jain,Iveta Sosova,Alicia Chan,Saadet Mercimek-Andrews
MOLECULAR GENETICS AND METABOLISM REPORTS (2024): 101055-101055
Silvia Radenkovic,Christin Johnsen,Andreas Schulze, Gurnoor Lail, Laura Guilder,Kaitlin Schwartz,Matthew Schultz,Saadet Mercimek-Andrews,Suzanne Boyer,Eva Morava
Therapeutic advances in rare disease (2023): 26330040221150269-263300402211502
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Crystal Mulik,Saadet Mercimek-Andrews
Turkish archives of pediatricsno. 2 (2023): 129-135
Thomas Klopstock,Saadet Mercimek-Andrews,Agnieszka Jurecka,Patricia Wood, Maciej Cwyl, Angelika Klucken,Antonio López,Roberta Scalise, Andrea Valle,Fatemeh Mollet,Belen Perez-Duenas, Marta Skowronska,
Orphanet journal of rare diseasesno. 1 (2023): 1-10
Apurba Mainali,Taryn Athey,Shalini Bahl, Clara Hung,Oana Caluseriu,Alicia Chan,Alison Eaton,Shailly Jain Ghai,Peter Kannu, Melissa MacPherson,Karen Y Niederhoffer,Komudi Siriwardena,
American journal of medical genetics. Part Ano. 2 (2023): 510-517
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