Michael M Khayat

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Dna Methylation

Intellectual Disability

Circulating Tumor Cells

Top Venues

Nature biotechnology

Journal of the National Cancer Institute

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

Publications

Varuna Chander, Medhat Mahmoud, Jianhong Hu, Zain Dardas, Christopher M Grochowski, Moez Dawood, Michael M Khayat, He Li, Shoudong Li, Shalini N. Jhangiani, Viktoriya Korchina, Hua Shen, George Weissenberger, Qingchang Meng, Marie-Claude Gingras, Donna M Muzny, Harsha Vardhan Doddapaneni, Jennifer E Posey, James R. Lupski, Aniko Sabo, David R Murdock, Fritz J Sedlazeck, Richard A Gibbs
Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism. Human mutation (2022)
He Li, Saumya Dushyant Sisoudiya, Bailey A Martin-Giacalone, Michael M Khayat, Shannon Dugan, Deborah A Marquez-Do, Michael E Scheurer, Donna Muzny, Eric Boerwinkle, Richard A Gibbs, Yueh-Yun Chi, Donald A Barkauskas, Tammy Lo, David C Hall, Douglas R Stewart, Joshua D Schiffman, Stephen X Skapek, Douglas S Hawkins, Sharon E Plon, Aniko Sabo, Philip J Lupo
Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology Group. Journal of the National Cancer Institute 113 (7) (2022)
Jonathan Foox, Scott W Tighe, Charles M Nicolet, Justin M Zook, Marta Byrska-Bishop, Wayne E Clarke, Michael M Khayat, Medhat Mahmoud, Phoebe K Laaguiby, Zachary T Herbert, Derek Warner, George S Grills, Jin Jen, Shawn E Levy, Jenny Xiang, Alicia Alonso, Xia Zhao, Wenwei Zhang, Fei Teng, Yonggang Zhao, Haorong Lu, Gary P Schroth, Giuseppe Narzisi, William Farmerie, Fritz J Sedlazeck, Don A Baldwin, Christopher E Mason
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nature biotechnology 39 (9) (2021)
Michael M Khayat, He Li, Varuna Chander, Jianhong Hu, Adam W Hansen, Shoudong Li, Josh Traynelis, Hua Shen, George Weissenberger, Fabio Stossi, Hannah L Johnson, James R. Lupski, Jennifer E Posey, Aniko Sabo, Qingchang Meng, David R Murdock, Michael Wangler, Richard A Gibbs
Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs syndrome. Human mutation 42 (5) (2021)
Ximena Montenegro-Garreaud, Adam W Hansen, Michael M Khayat, Varuna Chander, Christopher M Grochowski, Yunyun Jiang, He Li, Tadahiro Mitani, Elena Kessler, Joy Jayaseelan, Hua Shen, Alper Gezdirici, Davut Pehlivan, Qingchang Meng, Jill A Rosenfeld, Shalini N Jhangiani, Suneeta Madan-Khetarpal, Daryl A Scott, Hugo Abarca-Barriga, Milana Trubnykova, Marie-Claude Gingras, Donna M Muzny, Jennifer E Posey, Pengfei Liu, James R. Lupski, Richard A Gibbs
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases. Human mutation 41 (12) (2020)