Linyan Meng

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Botulinum Toxin

Top Venues

Annals of neurology

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill Anne Rosenfeld, Linyan Meng, Lindsay C Burrage, Michael F Wangler, Shinya Yamamoto, null null, Michael Santana, Victor Perez, Priyank Shukla, Christine M Eng, Brendan H Lee, Bo Yuan, Fan Xia, Hugo J Bellen, Pengfei Liu, Zhandong Liu
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI 1 (5) (2024)
Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill Anne Rosenfeld, Linyan Meng, Lindsay C Burrage, Michael F Wangler, Shinya Yamamoto, null null, Michael Santana, Victor Perez, Priyank Shukla, Christine M Eng, Brendan H Lee, Bo Yuan, Fan Xia, Hugo J Bellen, Pengfei Liu, Zhandong Liu
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI 1 (5) (2024)
Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill Anne Rosenfeld, Linyan Meng, Lindsay C Burrage, Michael F Wangler, Shinya Yamamoto, null null, Michael Santana, Victor Perez, Priyank Shukla, Christine M Eng, Brendan H Lee, Bo Yuan, Fan Xia, Hugo J Bellen, Pengfei Liu, Zhandong Liu
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI 1 (5) (2024)
Runjun D Kumar, Linyan Meng, Pengfei Liu, Christina Y Miyake, Kim C Worley, Weimin Bi, Seema R Lalani
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis. American journal of medical genetics. Part A 188 (11) (2022)
Linyan Meng, Pirjo Isohanni, Yunru Shao, Brett H Graham, Scott E Hickey, Stephanie Brooks, Anu Suomalainen, Pascal Joset, Katharina Steindl, Anita Rauch, Annette Hackenberg, Frances A High, Amy Armstrong-Javors, Niccolò E Mencacci, Paulina Gonzàlez-Latapi, Walaa A Kamel, Jasem Y Al-Hashel, Bernabé I Bustos, Alejandro V Hernandez, Dimitri Krainc, Steven J Lubbe, Hilde Van Esch, Chiara De Luca, Katleen Ballon, Claudia Ravelli, Lydie Burglen, Leila Qebibo, Daniel G Calame, Tadahiro Mitani, Dana Marafi, Davut Pehlivan, Nebal W Saadi, Yavuz Sahin, Reza Maroofian, Stephanie Efthymiou, Henry Houlden, Shazia Maqbool, Fatima Rahman, Shen Gu, Jennifer E Posey, James R Lupski, Jill V Hunter, Michael F Wangler, Christopher J Carroll, Yaping Yang
MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia. Annals of neurology 89 (4) (2021)
Dianalee McKnight, Lora Bean, Izabela Karbassi, Katelynn Beattie, Thierry Bienvenu, Hope Bonin, Ping Fang, John Chrisodoulou, Michael Friez, Maria Helgeson, Rahul Krishnaraj, Linyan Meng, Lindsey Mighion, Jeffrey Neul, Alan Percy, Simon Ramsden, Huda Zoghbi, Soma Das
Recommendations by the ClinGen Rett/Angelman-like expert panel for gene-specific variant interpretation methods. Human mutation (2021)
Marie Balzotti, Linyan Meng, Dale Muzzey, Katherine Johansen Taber, Kyle A Beauchamp, Myriad Genetics Curation Team, Baylor Genetics Curation Team, Rebecca Mar-Heyming, Bethany Buckley, Krista Moyer
Clinical validity of expanded carrier screening: Evaluating the gene-disease relationship in more than 200 conditions. Human mutation 41 (8) (2020)
Shen Gu, Chun-An Chen, Jill A Rosenfeld, Heidi Cope, Nathalie Launay, Kevin M Flanigan, Megan A Waldrop, Rachel Schrader, Jane Juusola, Ozlem Goker-Alpan, Aubrey Milunsky, Agatha Schlüter, Mónica Troncoso, Aurora Pujol, Queenie K-G Tan, Christian Patrick Schaaf, Linyan Meng
Truncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia. Human mutation 41 (3) (2019)