Chad A. Shaw - Concepedia

Author

Chad A. Shaw

Baylor College of Medicine ORCID

Also Known As

C A Shaw, C J Shaw, C Shaw, C. A. Shaw, C. J. Shaw, C. SHAW, C. Shaw, C.A. Shaw, C.J. Shaw, CA Shaw

400

Publications

28.3K

Citations

H-Index

241

Concepts

All Affiliations

Baylor College of Medicine Texas Children's Hospital Baylor Genetics Rice University Howard Hughes Medical Institute

About

Chad A. Shaw is an author at Baylor College of Medicine specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	60	95	15.3K
2	Public Health	12	13	1.5K
3	Health Sciences	9	9	2K
4	Natural Sciences	8	8	747
5	Engineering	7	7	308

Chad A. Shaw

199

Publications

26.3K

Citations

H-Index

Page 1

	Year	Citations
MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription Maria H. Chahrour, Sung Yun Jung, Chad A. Shaw, Science GeneticsMecp2 Gene CauseKey ContributorEpigeneticsSocial Sciences	2008	1.8K
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Neuron Neurodevelopmental DisordersWilliams Syndrome RegionSyndromic AutismGenetic DisorderGenetics	2011	1.3K
Aging Hematopoietic Stem Cells Decline in Function and Exhibit Epigenetic Dysregulation Stuart M. Chambers, Chad A. Shaw, Catherine E. Gatza, PLoS Biology AgingAdult Stem CellEpigeneticsTranscriptional RegulationLongevity	2007	791
A Protein–Protein Interaction Network for Human Inherited Ataxias and Disorders of Purkinje Cell Degeneration Janghoo Lim, Tong Hao, Chad A. Shaw, Cell Purkinje Cell DegenerationNeurodegenerative DiseasesMolecular NeuroscienceSynaptic SignalingGenetic Disorder	2006	787
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation Jennifer E. Posey, Tamar Harel, Pengfei Liu, New England Journal of Medicine	2016	752
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping Daniel A. Peiffer, Jennie Le, Frank J. Steemers, Genome Research	2006	538
The spliceosome is a therapeutic vulnerability in MYC-driven cancer Tiffany Hsu, Lukas M. Simon, Nicholas J. Neill, Nature Myc-driven CancerMedicineCancer GenomicsCancer GeneticsOncology	2015	510
A Renewable Tissue Resource of Phenotypically Stable, Biologically and Ethnically Diverse, Patient-Derived Human Breast Cancer Xenograft Models Xiaomei Zhang, Sofie Claerhout, Aleix Prat, Cancer Research	2013	470
A SUMOylation-Dependent Transcriptional Subprogram Is Required for Myc-Driven Tumorigenesis Jessica D. Kessler, Kristopher T. Kahle, Tingting Sun, Science Transcriptional RegulationSystems BiologyCell RegulationOncogenic AgentMedicine	2011	434
Characterization of Potocki-Lupski Syndrome (dup(17)(p11.2p11.2)) and Delineation of a Dosage-Sensitive Critical Interval That Can Convey an Autism Phenotype Lorraine Potocki, Weimin Bi, Diane Treadwell‐Deering, The American Journal of Human Genetics Neurodevelopmental DisordersAutism PhenotypePotocki-lupski SyndromePsychiatrySyndromic Autism	2007	425

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