Bryn D. Webb

2.0k citations

36 papers · 965 · h-index 14

Impact in

Molecular Biology
- Genomics and Chromatin Dynamics
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- RNA Research and Splicing
- Epigenetics and DNA Methylation
- Genomics and Phylogenetic Studies
- Mitochondrial Function and Pathology
Genetics top 10%

Papers in

Molecular Biology 17
- Mitochondrial Function and Pathology 5
- Cancer-related gene regulation 3
Genetics 13
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3

Co-authors: Ethylin Wang Jabs (12 shared papers)Mark J. Daly (1 shared paper)Gregory E. Crawford (1 shared paper)Daixing Zhou (1 shared paper)Ingeborg Holt (1 shared paper)John Bernat (1 shared paper)Shujun Luo (1 shared paper)Denise S. Tai (1 shared paper)
Journals: European Journal of Human Genetics (3 papers)Human Mutation (3 papers)Brain (2 papers)Clinical Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)
Partner nations: United States Germany Netherlands

In The Last Decade

Bryn D. Webb

32 papers receiving 937 citations

Peers

Countries citing papers authored by Bryn D. Webb

Since Specialization

Citations

This map shows the geographic impact of Bryn D. Webb'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 Bryn D. Webb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bryn D. Webb more than expected).

Fields of papers citing papers by Bryn D. Webb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bryn D. Webb. 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 Bryn D. Webb. The network helps show where Bryn D. Webb may publish in the future.

Co-authors

The 25 scholars most cited alongside Bryn D. Webb, 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 Bryn D. Webb Line = papers co-authored together Bryn D. Webb links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS) Genome Research ·Gregory E. Crawford, Ingeborg Holt, James R. Whittle, Bryn D. Webb, Denise S. Tai, Sean Davis, Elliott H. Margulies, YiDong Chen, John Bernat, David Ginsburg, Daixing Zhou, Shujun Luo, Thomas J. Vasicek, Mark J. Daly, Tyra G. Wolfsberg, Francis S. Collins	2005	381
2	A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3 Brain ·Sheena Chew, Ravikumar Balasubramanian, Wai‐Man Chan, Peter B. Kang, Caroline Andrews, Bryn D. Webb, Sarah MacKinnon, Darren T. Oystreck, Jessica K. Rankin, Thomas O. Crawford, Michael T. Geraghty, Scott L. Pomeroy, William F. Crowley, Ethylin Wang Jabs, David G. Hunter, P. Ellen Grant, Elizabeth C. Engle	2013	90
3	Complex Autoinflammatory Syndrome Unveils Fundamental Principles of JAK1 Kinase Transcriptional and Biochemical Function Immunity ·Conor Gruber, Jorg J. A. Calis, Sofija Buta, Gilad D. Evrony, J.P. Martin, Skyler Uhl, Rachel Caron, Lauren Jarchin, David Dunkin, Robert Phelps, Bryn D. Webb, Jeffrey M. Saland, Miriam Mérad, Jordan S. Orange, Emily M. Mace, Brad R. Rosenberg, Bruce D. Gelb, Dusan Bogunovic	2020	86
4	HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice The American Journal of Human Genetics ·Bryn D. Webb, Sherin Shaaban, Harald Gaspar, Luis F. Cunha, Christian Schubert, Ke Hao, Caroline D. Robson, Wai‐Man Chan, Caroline Andrews, Sarah MacKinnon, Darren T. Oystreck, David G. Hunter, Anthony J. Iacovelli, Xiaoqian Ye, Anne Camminady, Elizabeth C. Engle, Ethylin Wang Jabs	2012	61
5	Deficiency of the alkaline ceramidase ACER3 manifests in early childhood by progressive leukodystrophy Journal of Medical Genetics ·Simon Edvardson, Jae Kyo Yi, Chaim Jalas, Ruijuan Xu, Bryn D. Webb, Justin M. Snider, Anastasia Fedick, (unknown), Nathan R. Treff, Cungui Mao, Orly Elpeleg	2016	43
6	Quantitative Assessment of Facial Asymmetry Using Three-Dimensional Surface Imaging in Adults: Validating the Precision and Repeatability of a Global Approach The Cleft Palate-Craniofacial Journal ·Davida Kornreich, Adele A. Mitchell, Bryn D. Webb, Ingrid Cristian, Ethylin Wang Jabs	2014	31
7	Identification of STAC3 variants in non‐Native American families with overlapping features of Carey–Fineman–Ziter syndrome and Moebius syndrome American Journal of Medical Genetics Part A ·Aida Telegrafi, Bryn D. Webb, Sarah Poll, Carlos E. Speck‐Martins, David Fitzpatrick, Leah Fleming, Richard J. Redett, Andreas Dufke, Gunnar Houge, J. J. T. van Harssel, Alain Verloès, Angela Robles, Irini Manoli, Elizabeth C. Engle, Ethylin Wang Jabs, David Valle, John C. Carey, Julie Hoover‐Fong, Nara L. M. Sobreira	2017	29
8	Novel, Compound Heterozygous, Single-Nucleotide Variants inMARS2Associated with Developmental Delay, Poor Growth, and Sensorineural Hearing Loss Human Mutation ·Bryn D. Webb, Patricia G. Wheeler, Jacob Hagen, Ninette Cohen, Michael D. Linderman, George A. Díaz, Thomas P. Naidich, Richard J. Rodenburg, Sander M. Houten, Eric E. Schadt	2015	28
9	Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease‐causing variants Clinical Genetics ·Lijun Shi, Bryn D. Webb, Ashley H. Birch, Lama Elkhoury, Janelle McCarthy, Xiaoqiang Cai, Kimihiko Oishi, Lakshmi Mehta, George A. Diaz, Lisa Edelmann, Ruth Kornreich	2016	21
10	Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes Brain ·Janet C. Rucker, Bryn D. Webb, Tamiesha Frempong, Harald Gaspar, Thomas P. Naidich, Ethylin Wang Jabs	2014	19
11	Heterozygous Pathogenic Variant inDACT1Causes an Autosomal-Dominant Syndrome with Features Overlapping Townes-Brocks Syndrome Human Mutation ·Bryn D. Webb, Sanjeeva Metikala, Patricia G. Wheeler, Mingma D. Sherpa, Sander M. Houten, Marko E. Horb, Eric E. Schadt	2017	17
12	Mitochondrial translation defects and human disease PubMed ·Bryn D. Webb, George A. Díaz, Pankaj Prasun	2020	16
13	Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis European Journal of Human Genetics ·Bryn D. Webb, Hilary Hotchkiss, Pankaj Prasun, Bruce D. Gelb, Lisa M. Satlin	2021	14
14	A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population Clinical Genetics ·Bryn D. Webb, Tracy Brandt, L. Liu, Chaim Jalas, Jun Liao, Anastasia Fedick, Michael D. Linderman, George A. Díaz, Ruth Kornreich, Howard Trachtman, Lakshmi Mehta, Lisa Edelmann	2013	13
15	Lessons learned from expanded reproductive carrier screening in self‐reported Ashkenazi, Sephardi, and Mizrahi Jewish patients Molecular Genetics & Genomic Medicine ·Gidon Akler, Ashley H. Birch, Nicole Schreiber‐Agus, Xiaoqiang Cai, Guiqing Cai, Lisong Shi, Chunli Yu, Anastasia M. Larmore, Geetu Mendiratta‐Vij, Lama Elkhoury, Mitchell W. Dillon, Jun Zhu, Andrew McLellan, Funda Suer, Bryn D. Webb, Eric E. Schadt, Ruth Kornreich, Lisa Edelmann	2019	12
16	Missense NAA20 variantsimpairing the NatB protein N-terminal acetyltransferase cause autosomal recessivedevelopmental delay, intellectual disability, and microcephaly Genetics in Medicine ·Jennifer Morrison, Norah K. Altuwaijri, Kirsten Brønstad, Henriette Aksnes, Hessa S. Alsaif, Anthony Evans, (unknown), Patricia G. Wheeler, Bryn D. Webb, Fowzan S. Alkuraya, Thomas Arnesen	2021	12
17	Identification of a novel pathogenic <em>OTOF</em> variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population The Application of Clinical Genetics ·Bryn D. Webb, Anastasia Fedick, Chaim Jalas, Ananya Swaroop, Eric Smouha	2016	12
18	DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients European Journal of Human Genetics ·Roser Urreizti, Klaus Mayer, Gilad D. Evrony, Edith Said, Laura Castilla‐Vallmanya, Neal Cody, Guillem Plasencia, Bruce D. Gelb, Daniel Grinberg, Ulrich Brinkmann, Bryn D. Webb, (unknown)	2019	12
19	Haploinsufficiency of the basic helix–loop–helix transcription factorHAND2causes congenital heart defects American Journal of Medical Genetics Part A ·Ana S.A. Cohen, Christopher Simotas, Bryn D. Webb, Huanzhi Shi, Wahab Khan, Lisa Edelmann, Stuart A. Scott, Ram J. Singh	2020	10
20	Mirror Movements Identified in Patients with Moebius Syndrome PubMed ·Bryn D. Webb, Tamiesha Frempong, Thomas P. Naidich, Harald Gaspar, Ethylin Wang Jabs, Janet C. Rucker	2014	8

About Bryn D. Webb

Bryn D. Webb is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Neurology and Pathology and Forensic Medicine, having authored 36 papers that have together received 965 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (5 papers), Facial Nerve Paralysis Treatment and Research (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Cancer-related gene regulation (3 papers) and Trigeminal Neuralgia and Treatments (3 papers). The work is most often cited by research in Molecular Biology (574 citations), Genetics (202 citations), Anatomy (7 citations), Cancer Research (54 citations) and Sensory Systems (18 citations). Bryn D. Webb has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Ethylin Wang Jabs, Mark J. Daly, Gregory E. Crawford, Daixing Zhou, Ingeborg Holt, John Bernat, Shujun Luo, Denise S. Tai, Thomas J. Vasicek and James R. Whittle. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Brain, Clinical Genetics and Orphanet Journal of Rare Diseases.

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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Bryn D. Webb

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