Michael M. Khayat - Concepedia

Author

Michael M. Khayat

Also Known As

J. Thomas Kolar, Khayat, Michael M., MICHAEL M. KHAYAT, Michael Khayat, Michael M Khayat, Michael M. Khayat, Ximena Montenegro-Garreaud

Publications

765

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine Texas Children's Hospital Baylor Genetics The University of Texas Health Science Center at Houston Neurological Research Institute

About

Michael M. Khayat is an author at Baylor College of Medicine specializing in genetics, medicine, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	244
2	Natural Sciences	1	1	14
3	Public Health	1	1	33
4	Microbiology	1	1	145
5	Molecular Biology	1	1	14

Michael M. Khayat

Publications

654

Citations

H-Index

Page 1

	Year	Citations
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study Jonathan Foox, Scott Tighe, Charles M. Nicolet, Nature Biotechnology Long-read SequencingDna SequencingFunctional GenomicsSequencingMolecular Ecology	2021	145
<b>Germline Cancer Predisposition Variants in</b> <b>Pediatric Rhabdomyosarcoma: A Report From the Children’s Oncology Group</b> He Li, Saumya D. Sisoudiya, Bailey A. Martin‐Giacalone, JNCI Journal of the National Cancer Institute	2020	99
Phenotypic expansion in <i> <scp>DDX</scp> 3X </i> – a common cause of intellectual disability in females Xia Wang, Jennifer E. Posey, Jill A. Rosenfeld, Annals of Clinical and Translational Neurology	2018	86
Exome variant discrepancies due to reference-genome differences Li He, Moez Dawood, Michael M. Khayat, The American Journal of Human Genetics Allelic VariantExome Variant DiscrepanciesGeneticsGenome AnalysisGenetic Variation	2021	63
The phenotypic spectrum of Xia‐Gibbs syndrome Yunyun Jiang, Michael F. Wangler, Amy L. McGuire, American Journal of Medical Genetics Part A	2018	48
Hidden biases in germline structural variant detection Michael M. Khayat, Sayed Mohammad Ebrahim Sahraeian, Samantha Zarate, Genome biology	2021	39
A Universal Next-Generation Sequencing Protocol To Generate Noninfectious Barcoded cDNA Libraries from High-Containment RNA Viruses Lindsey A. Moser, Lisbeth Ramírez-Carvajal, Vinita Puri, mSystems	2016	33
A Genocentric Approach to Discovery of Mendelian Disorders Adam Hansen, Mullai Murugan, He Li, The American Journal of Human Genetics Mendelian DisorderGenocentric ApproachGenetic DisorderGeneticsGenetic Epidemiology	2019	33
Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition David R. Murdock, Yunyun Jiang, Michael F. Wangler, Molecular Case Studies	2019	23
Phenotypic and protein localization heterogeneity associated with <i>AHDC1</i> pathogenic protein‐truncating alleles in Xia–Gibbs syndrome Michael M. Khayat, He Li, Varuna Chander, Human Mutation GeneticsMotor DevelopmentPathologyMolecular GeneticsDisease Gene Identification	2021	22

Page 1