Bryn D. Webb

1.9k citations

35 papers · 896 indexed · h-index 13

Molecular Biology
- Mitochondrial Function and Pathology 4
- Cancer-related gene regulation 3
- RNA modifications and cancer 3
Genetics top 10%
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
Orthodontics
Genetics
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
Cancer Research
Neurology
- Facial Nerve Paralysis Treatment and Research 6
Clinical Biochemistry
- Metabolism and Genetic Disorders 5
Pathology and Forensic Medicine
- Trigeminal Neuralgia and Treatments 3

Co-authors: Sean Davis Daixing Zhou Tyra G. Wolfsberg James R. Whittle Ingeborg Holt Francis S. Collins David Ginsburg Mark J. Daly
Cited by: Molecular Biology Genetics Orthodontics
Journals: European Journal of Human Genetics (3 papers)Human Mutation (3 papers)Orphanet Journal of Rare Diseases (2 papers)
Partner nations: United States Germany Netherlands

In The Last Decade

Bryn D. Webb

31 papers receiving 880 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-authorship network

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

#	Work
1	An algorithm to identify patients aged 0–3 with rare genetic disorders Orphanet Journal of Rare Diseases ·Bryn D. Webb,高宗文,Sana Iqbal,Xi Chen,D Corrigan,Lisong Shi,Seungwoo Lee,Barbora Hrdová Kolíbalová,Shilong Li,Zichen Wang,Cynthia A. Vokoun,Lisa Edelmann,Rong Chen,Eric E. Schadt,Li Li	2024	0
2	Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia American Journal of Medical Genetics Part A ·Behzad Pourmokhtari,Bryn D. Webb,Lisa Edelmann,Jun Liao,Lakshmi Mehta	2024	0
3	Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness International Journal of Environmental Research and Public Health ·Denise K. Liberton,Konstantinia Almpani,Rashmi Mishra,Carol W. Bassim,Carol Van Ryzin,Bryn D. Webb,Ethylin Wang Jabs,Elizabeth C. Engle,Francis S. Collins,Irini Manoli,Janice S. Lee	2024	0
4	Inability to move one's face dampens facial expression perception Cortex ·Shruti Japee,Jessica Jordan,Manuel Llorente Vazquez,Vladimir N. Safonov,Gang Chen,Joseph Snow,Ethylin Wang Jabs,Bryn D. Webb,Elizabeth C. Engle,Irini Manoli,Chris I. Baker,Leslie G. Ungerleider	2023	5
5	Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency eLife ·Bryn D. Webb,Sara M. Nowinski,Ashley Solmonson,Jaya Ganesh,Richard J. Rodenburg,João Leandro,Anggun Puspita Hapsari,Hieu Vu,Thomas P. Naidich,Bruce D. Gelb,Ralph J. DeBerardinis,Jared Rutter,Sander M. Houten	2023	4
6	Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor Human Mutation ·Bryn D. Webb,Anggun Puspita Hapsari,Thomas P. Naidich,Lynne M. Bird,Sumit Parikh,Meilín Fernández García,Lindsay B. Henderson,Francisca Millan,Yue Si,Kristen Brennand,Peter Shih-Ping Hung,Janet C. Rucker,Patricia G. Wheeler,Eric E. Schadt	2021	0
7	Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies Muscle & Nerve ·Tanya Lehky,Min-Min Qian,Camilo Toro,Tianxia Wu,Carol Van Ryzin,Andrea Gropman,Flavia M. Facio,Bryn D. Webb,Ethylin Wang Jabs,J Purkyně,Elizabeth C. Engle,Francis S. Collins,Irini Manoli	2021	4
8	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	13
9	Mitochondrial translation defects and human disease PubMed ·Bryn D. Webb,George A. Díaz,Pankaj Prasun	2020	15
10	Haploinsufficiency of the basic helix–loop–helix transcription factorHAND2causes congenital heart defects American Journal of Medical Genetics Part A ·Ana S.A. Cohen,P. H. Meller,Bryn D. Webb,C.A.J. Vlek,Wahab Khan,Lisa Edelmann,Stuart A. Scott,Ram J. Singh	2020	10
11	Correction: 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,K. Ulrich Mayer,Gilad D. Evrony,Edith Said,А.А. ВЕРНИГОРА,Neal Cody,Carina Vance,Bruce D. Gelb,Daniel Grinberg,Ulrich Brinkmann,Bryn D. Webb,Susana Balcells	2019	1
12	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,А.А. ВЕРНИГОРА,Neal Cody,Carina Vance,Bruce D. Gelb,Daniel Grinberg,Ulrich Brinkmann,Bryn D. Webb,Susana Balcells	2019	12
13	Heterozygous Pathogenic Variant inDACT1Causes an Autosomal-Dominant Syndrome with Features Overlapping Townes-Brocks Syndrome Human Mutation ·Bryn D. Webb,全哉當山,Patricia G. Wheeler,真理端野,Sander M. Houten,Marko E. Horb,Eric E. Schadt	2017	17
14	ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories Genome Medicine ·Jinlian Wang,Jun Liao,Jinglan Zhang,Wei‐Yi Cheng,Jörg Hakenberg,Meng Ma,Bryn D. Webb,Zhouhao Wang,Behzad Pourmokhtari,Lakshmi Mehta,Ruth Kornreich,George A. Díaz,Shuyu Li,Lisa Edelmann,Rong Chen	2015	5
15	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	12
16	Evaluation of the Affymetrix CytoScan^®Dx Assay for developmental delay Expert Review of Molecular Diagnostics ·Bryn D. Webb,Rebecca J. Scharf,Daryl L. Harris,Lisa Edelmann,Annemarie Stroustrup	2014	6
17	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	81
18	Determinants of quality of life in children with chronic somatic disease: pilot data from the GapS Questionnaire Quality of Life Research ·Bryn D. Webb,Maru Barrera,Joseph Beyene,Manuel Carção,Denis Daneman,Irene Elliott,Tomeka Kim,Ilana Halperin,谭劼,Hilary Chan,Unni Narayanan,S. Ota,Melinda Solomon,Lillian Sung,Nancy L. Young,Mary Zachos,Brian M. Feldman	2012	4
19	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,ノボルシオミ,Elizabeth C. Engle,Ethylin Wang Jabs	2012	53
20	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,JinChun Li,John Bernat,David Ginsburg,Daixing Zhou,Shujun Luo,Thomas J. Vasicek,Mark J. Daly,Tyra G. Wolfsberg,Francis S. Collins	2005	368

About Bryn D. Webb

Bryn D. Webb is a scholar working on Clinical Biochemistry, Genetics and Complementary and Manual Therapy, having authored 35 papers that have together received 896 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Facial Nerve Paralysis Treatment and Research (6 papers), Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer-related gene regulation (3 papers), Trigeminal Neuralgia and Treatments (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Molecular Biology (588 citations), Genetics (212 citations) and Orthodontics (19 citations). Bryn D. Webb has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Sean Davis, Daixing Zhou, Tyra G. Wolfsberg, James R. Whittle, Ingeborg Holt, Francis S. Collins, David Ginsburg, Mark J. Daly, Gregory E. Crawford and Shujun Luo. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Orphanet Journal of Rare Diseases, Brain and Clinical 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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