Chad A. Shaw

28.5k citations

193 papers · 13.9k indexed · 3 hit papers · h-index 65

Impact in

Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Aging top 0.5%

Papers in

Aging 6
Genetics 91
- Genomic variations and chromosomal abnormalities 59
- Genomics and Rare Diseases 25
- Genetics and Neurodevelopmental Disorders 18

Co-authors: Huda Y. Zoghbi James R. Lupski Maria H. Chahrour Jun Qin Stephen T.C. Wong Xiaobo Zhou Sung Yun Jung Paweł Stankiewicz
Journals: PLoS Genetics (10 papers)Blood (9 papers)Human Molecular Genetics (9 papers)The American Journal of Human Genetics (8 papers)European Journal of Human Genetics (7 papers)
Partner nations: United States Canada Poland

In The Last Decade

Chad A. Shaw

191 papers receiving 13.6k citations

Hit Papers

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MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription 2008 · 1.4k citations

Peers

Countries citing papers authored by Chad A. Shaw

Since Specialization

Citations

This map shows the geographic impact of Chad A. Shaw's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Chad A. Shaw with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chad A. Shaw more than expected).

Fields of papers citing papers by Chad A. Shaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chad A. Shaw. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Chad A. Shaw. The network helps show where Chad A. Shaw may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Chad A. Shaw, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Chad A. Shaw Line = papers co-authored together Chad A. Shaw links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits Genome Medicine ·Bo Yuan, Naveen Kandpal, Nurit Assia Batzir, Valentina Álvarez-Flórez, Hongzheng Dai, Wenmiao Zhu, 湯浅文雄, Chin‐To Fong, J. Lloyd Holder, Joanne Nguyen, Christian P. Schaaf, Yaping Yang, Weimin Bi, Christine M. Eng, Chad A. Shaw, James R. Lupski, Pengfei Liu	2022	2
2	Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH Journal of Medical Genetics ·Subramaniam Sundaramahalingam, Ian M. Campbell, Andrés Hernández, Seema R. Lalani, Pengfei Liu, Chad A. Shaw, Jill A. Rosenfeld, Daryl A. Scott	2021	21
3	Bayesian modelling of high-throughput sequencing assays with malacoda PLoS Computational Biology ·Andrew R. Ghazi, Xianguo Kong, Michael Strueber, Leonard C. Edelstein, Chad A. Shaw	2020	3
4	Functionalization of CD36 cardiovascular disease and expression associated variants by interdisciplinary high throughput analysis PLoS Genetics ·Louis Hogrefe, Andrew R. Ghazi, Xianguo Kong, Edward S. Chen, Chad A. Shaw, Leonard C. Edelstein	2019	8
5	Global Gene Expression Profiling in Infants With Acute Respiratory Syncytial Virus Broncholitis Demonstrates Systemic Activation of Interferon Signaling Networks The Pediatric Infectious Disease Journal ·Kristine L Bucasas, Asad Mian, Gail J. Demmler‐Harrison, A. Chantal Caviness, Pedro A. Piedra, Luis M. Franco, Chad A. Shaw, Patrice Winder, Xueqing Wang, Molly S. Bray, Robert B. Couch, John W. Belmont	2012	27
6	Incidental copy-number variants identified by routine genome testing in a clinical population Genetics in Medicine ·Philip M. Boone, Zachry T. Soens, Ian M. Campbell, Paweł Stankiewicz, Sau Wai Cheung, Ankita Patel, Arthur L. Beaudet, Sharon E. Plon, Chad A. Shaw, Amy L. McGuire, James R. Lupski	2012	30
7	Proinflammatory Role for let-7 MicroRNAS in Experimental Asthma Journal of Biological Chemistry ·Sumanth Polikepahad, John Knight, A.O. Naghavi, Jianqiang Sun, Chad J. Creighton, Chad A. Shaw, Ashley Benham, Jong Kim, Benjamin Soibam, R. Alan Harris, Cristian Coarfa, Azam Zariff, Aleksandar Milosavljevic, R. DeC. Ward, Farrah Kheradmand, Preethi H. Gunaratne, David B. Corry	2010	200
8	Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia Human Molecular Genetics ·Juliette J. Kahle, Natali Gulbahce, Chad A. Shaw, Janghoo Lim, David E. Hill, Albert-Ĺaszló Barabási, Huda Y. Zoghbi	2010	37
9	Array Comparative Genomic Hybridization Detects Chromosomal Abnormalities in Hematological Cancers That Are Not Detected by Conventional Cytogenetics Journal of Molecular Diagnostics ·Lina Shao, Sung-Hae L. Kang, Jian Li, Patricia Hixson, Mikaela Malm, Svetlana A. Yatsenko, Chad A. Shaw, Aleksandar Milosavljevic, Chung-Che Chang, Sau Wai Cheung, Ankita Patel	2010	18
10	VAMP8/endobrevin is overexpressed in hyperreactive human platelets: suggested role for platelet microRNA Journal of Thrombosis and Haemostasis ·Altaf A. Kondkar, Molly S. Bray, Suzanne M. Leal, Srinivasa R. Nagalla, Adam Brejtfus, Ying Jin, Jing Dong, Bitupon Boruah, Sidney W. Whiteheart, Chad A. Shaw, Paul F. Bray	2009	156
11	Application of dual-genome oligonucleotidearray-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes Genetics in Medicine ·A. Craig Chinault, Chad A. Shaw, Ellen K. Brundage, Lin-ya Tang, Lee‐Jun C. Wong	2009	40
12	MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription Science ·Maria H. Chahrour, Sung Yun Jung, Chad A. Shaw, Xiaobo Zhou, Stephen T.C. Wong, Jun Qin, Huda Y. Zoghbi Hit paper breakdown →	2008	1372
13	Mouse let-7 miRNA populations exhibit RNA editing that is constrained in the 5′-seed/ cleavage/anchor regions and stabilize predicted mmu-let-7a:mRNA duplexes Genome Research ·Jeffrey G. Reid, Ankur K. Nagaraja, Francis C. Lynn, Rafal Drabek, Donna M. Muzny, Chad A. Shaw, Ingrid Jesus dos Santos, A.O. Naghavi, Fiche réalisée en partenariat avec la Mnh, Huifeng Zhu, Jayantha B. Tennakoon, Gemunu H. Gunaratne, David B. Corry, Jonathan Miller, Michael T. McManus, Michael S. German, Richard A. Gibbs, Martin M. Matzuk, Preethi H. Gunaratne	2008	73
14	22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome The American Journal of Human Genetics ·Shay Ben‐Shachar, Zhishuo Ou, Chad A. Shaw, John W. Belmont, Millan S. Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan S. Berg, V. Reid Sutton, Seema R. Lalani, A. Craig Chinault, Sau Wai Cheung, James R. Lupski, Ankita Patel	2008	142
15	Aging Hematopoietic Stem Cells Decline in Function and Exhibit Epigenetic Dysregulation PLoS Biology ·Stuart M. Chambers, Chad A. Shaw, Catherine E. Gatza, Παντελεήμων Λιβανός, Lawrence A. Donehower, Margaret A. Goodell Hit paper breakdown →	2007	580
16	Lithium Therapy Improves Neurological Function and Hippocampal Dendritic Arborization in a Spinocerebellar Ataxia Type 1 Mouse Model PLoS Medicine ·Kei Watase, Jennifer R. Gatchel, Yaling Sun, Effat S. Emamian, Richard Atkinson, Ronald Richman, Hidehiro Mizusawa, Harry T. Orr, Chad A. Shaw, Huda Y. Zoghbi	2007	128
17	Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease Human Molecular Genetics ·Jennifer A. Lee, Ken Inoue, Sau Wai Cheung, Chad A. Shaw, Paweł Stankiewicz, James R. Lupski	2006	56
18	Molecular Signatures of Proliferation and Quiescence in Hematopoietic Stem Cells PLoS Biology ·和博西村, Akil Merchant, Carlos A. Ramos, З. А. Тогузова, Andrew Young, Chad A. Shaw, Margaret A. Goodell	2004	266
19	Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure European Journal of Human Genetics ·Marzena Gajęcka, Wei Yu, Blake C. Ballif, Caron D. Glotzbach, Guddeti Rama Thulasi Reddy, Chad A. Shaw, Catherine D. Kashork, Heidi A. Heilstedt, Hang Yuan, Aaron Theisen, Ritva Rice, David Rice, Lisa G. Shaffer	2004	68
20	An Accurate, Sensitive, and Scalable Method to Identify Functional Sites in Protein Structures Journal of Molecular Biology ·Hui Yao, David M. Kristensen, Ivana Mihalek, Mathew E. Sowa, Chad A. Shaw, Marek Kimmel, Lydia E. Kavraki, Olivier Lichtarge	2003	149

About Chad A. Shaw

Chad A. Shaw is a scholar working on Aging, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 193 papers that have together received 13.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (59 papers), Genomics and Rare Diseases (25 papers), Prenatal Screening and Diagnostics (24 papers), Chromosomal and Genetic Variations (21 papers), Genetics and Neurodevelopmental Disorders (18 papers), Congenital heart defects research (17 papers), Epigenetics and DNA Methylation (11 papers) and Genetic Neurodegenerative Diseases (10 papers). The work is most often cited by research in Genetics (5.7k citations), Aging (354 citations), Molecular Biology (7.7k citations), Cancer Research (1.5k citations) and Hematology (1.1k citations). Chad A. Shaw has collaborated with scholars based in United States, Canada and Poland. Frequent co-authors include Huda Y. Zoghbi, James R. Lupski, Maria H. Chahrour, Jun Qin, Stephen T.C. Wong, Xiaobo Zhou, Sung Yun Jung, Paweł Stankiewicz, Sau Wai Cheung and Margaret A. Goodell. Their work appears in journals such as PLoS Genetics, Blood, Human Molecular Genetics, The American Journal of Human Genetics and European Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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