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个人简介
I feel fortunate to have led several wonderful collaborative teams on clinical laboratory operation, bioinformatics, NGS R&D, and genomics interpretation/reporting service. The efforts have brought rapid whole genome sequencing, exome sequencing, expanded carrier screening, single-gene NIPT and oncology tests as clinical offerings in Baylor Genetics.
I am ABMGG board-certified in clinical molecular genetics. I am passionate about applying advanced molecular genomics technologies into applications. I am also a faculty member in the department of molecular and human genetics at Baylor College of Medicine. My research focuses on the neurological and developmental disorders. I have been mentoring fellows of ABMGG training programs.
I am ABMGG board-certified in clinical molecular genetics. I am passionate about applying advanced molecular genomics technologies into applications. I am also a faculty member in the department of molecular and human genetics at Baylor College of Medicine. My research focuses on the neurological and developmental disorders. I have been mentoring fellows of ABMGG training programs.
研究兴趣
论文共 118 篇作者统计合作学者相似作者
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AMERICAN JOURNAL OF HUMAN GENETICSno. 2 (2024): 364-382
Amir Hossein Saeidian,Liesbeth Vossaert,Elizabeth Mizerik, Wilson CW. Wu,Hongzheng Dai,Nichole Owen,Janice Smith,Linyan Meng,Christine Eng,Fan Xia,Weimin Bi,Xiaonan Zhao
Genetics in Medicine Open (2024): 101586
Dongxue Mao,Chaozhong Liu,Linhua Wang, Rami Ai-Ouran,Cole Deisseroth, Sasidhar Pasupuleti,Seon Young Kim,Lucian Li,Jill A Rosenfeld,Linyan Meng,Lindsay C Burrage,Michael F Wangler,
NEJM AIno. 5 (2024)
Alistair T Pagnamenta, Rebecca S Belles,Bonnie Anne Salbert,Ingrid M Wentzensen,Maria J Guillen Sacoto,Francis Jeshira Reynoso Santos,Alesky Caffo,Matteo Ferla,Benito Banos-Pinero, Karolina Pawliczak, Mina Makvand,Hossein Najmabadi,
Linyan Meng,Ruben Attali,Tomer Talmy, Yakir Regev, Niv Mizrahi,Pola Smirin-Yosef,Liesbeth Vossaert,Christian Taborda,Michael Santana,Ido Machol,Rui Xiao,Hongzheng Dai,
Genetics in Medicineno. 3 (2022): S263-S264
Genetics in Medicineno. 3 (2022): S210-S211
Genetics in Medicineno. 3 (2022): S301-S301
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