Michael M Khayat

6PUBLICATIONS
38CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Sequence analysisHaematological tumoursCancer geneticsNeurology and neuromuscular diseases
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Publications (6)

|Sep 02, 2022
Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism.

Varuna Chander, Medhat Mahmoud, Jianhong Hu

|Oct 12, 2021
Author Correction: Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study.

Jonathan Foox, Scott W Tighe, Charles M Nicolet

|Sep 10, 2021
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study.

Jonathan Foox, Scott W Tighe, Charles M Nicolet

|Mar 01, 2021
Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs syndrome.

Michael M Khayat, He Li, Varuna Chander

|Dec 29, 2020
Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology Group.

He Li, Saumya D Sisoudiya, Bailey A Martin-Giacalone

|Sep 16, 2020
Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases.

Ximena Montenegro-Garreaud, Adam W Hansen, Michael M Khayat

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Frequent Collaborators

3 joint publications

Fritz J Sedlazeck

3 joint publications

Jennifer E Posey

3 joint publications

James R Lupski

3 joint publications

He Li