Bryn D. Webb

1.9k total citations
35 papers, 896 citations indexed

About

Bryn D. Webb is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Bryn D. Webb has authored 35 papers receiving a total of 896 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Neurology. Recurrent topics in Bryn D. Webb's work include Genomics and Rare Diseases (7 papers), Facial Nerve Paralysis Treatment and Research (6 papers) and Metabolism and Genetic Disorders (5 papers). Bryn D. Webb is often cited by papers focused on Genomics and Rare Diseases (7 papers), Facial Nerve Paralysis Treatment and Research (6 papers) and Metabolism and Genetic Disorders (5 papers). Bryn D. Webb collaborates with scholars based in United States, Germany and Netherlands. Bryn D. Webb's co-authors include John Bernat, Ingeborg Holt, David Ginsburg, Shujun Luo, Tyra G. Wolfsberg, Daixing Zhou, Thomas J. Vasicek, Mark J. Daly, Elliott H. Margulies and Francis S. Collins and has published in prestigious journals such as SHILAP Revista de lepidopterología, Immunity and Brain.

In The Last Decade

Bryn D. Webb

31 papers receiving 880 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Bryn D. Webb United States 13 588 212 78 71 60 35 896
Jean‐Pierre Desvignes France 17 603 1.0× 324 1.5× 52 0.7× 37 0.5× 72 1.2× 31 1.0k
Jiong Yan United States 15 650 1.1× 487 2.3× 92 1.2× 46 0.6× 56 0.9× 27 1.0k
Tomoko Uehara Japan 14 358 0.6× 275 1.3× 82 1.1× 69 1.0× 34 0.6× 79 733
Nisha Patel Saudi Arabia 17 428 0.7× 267 1.3× 59 0.8× 53 0.7× 60 1.0× 39 727
Pagon Ra United States 6 450 0.8× 260 1.2× 86 1.1× 55 0.8× 23 0.4× 291 791
Tatsuaki Kurosaki United States 13 1.1k 1.8× 211 1.0× 63 0.8× 30 0.4× 109 1.8× 24 1.3k
Aaron Mammoser United States 11 462 0.8× 225 1.1× 56 0.7× 35 0.5× 58 1.0× 25 765
David B. Everman United States 20 657 1.1× 466 2.2× 42 0.5× 61 0.9× 51 0.8× 39 1.1k
Jason A. Watts United States 12 862 1.5× 144 0.7× 67 0.9× 74 1.0× 87 1.4× 21 1.0k
Boris Keren France 21 649 1.1× 515 2.4× 115 1.5× 44 0.6× 29 0.5× 70 1.1k

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 of co-authors of Bryn D. Webb

This figure shows the co-authorship network connecting the top 25 collaborators of Bryn D. Webb. A scholar is included among the top collaborators of Bryn D. Webb based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bryn D. Webb. Bryn D. Webb is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Webb, Bryn D., D Corrigan, Lisong Shi, et al.. (2024). An algorithm to identify patients aged 0–3 with rare genetic disorders. Orphanet Journal of Rare Diseases. 19(1). 183–183.
2.
Webb, Bryn D., et al.. (2024). Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia. American Journal of Medical Genetics Part A. 197(5). e63954–e63954.
3.
Liberton, Denise K., Konstantinia Almpani, Rashmi Mishra, et al.. (2024). Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness. International Journal of Environmental Research and Public Health. 21(5). 615–615.
4.
Webb, Bryn D., Sara M. Nowinski, Ashley Solmonson, et al.. (2023). Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency. eLife. 12. 4 indexed citations
5.
Japee, Shruti, Jessica Jordan, Gang Chen, et al.. (2023). Inability to move one's face dampens facial expression perception. Cortex. 169. 35–49. 5 indexed citations
6.
Webb, Bryn D., Thomas P. Naidich, Lynne M. Bird, et al.. (2021). Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor. Human Mutation. 42(6). 685–693.
7.
Lehky, Tanya, Camilo Toro, Tianxia Wu, et al.. (2021). Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies. Muscle & Nerve. 63(4). 516–524. 4 indexed citations
8.
Cohen, Ana S.A., Bryn D. Webb, Wahab Khan, et al.. (2020). Haploinsufficiency of the basic helix–loop–helix transcription factorHAND2causes congenital heart defects. American Journal of Medical Genetics Part A. 182(5). 1263–1267. 10 indexed citations
9.
Webb, Bryn D., George A. Díaz, & Pankaj Prasun. (2020). Mitochondrial translation defects and human disease. PubMed. 4. 71–80. 15 indexed citations
10.
Urreizti, Roser, Klaus Mayer, Gilad D. Evrony, et al.. (2019). DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients. European Journal of Human Genetics. 28(1). 64–75. 12 indexed citations
11.
Urreizti, Roser, K. Ulrich Mayer, Gilad D. Evrony, et al.. (2019). Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients. European Journal of Human Genetics. 28(1). 138–138. 1 indexed citations
12.
Webb, Bryn D., et al.. (2017). Heterozygous Pathogenic Variant inDACT1Causes an Autosomal-Dominant Syndrome with Features Overlapping Townes-Brocks Syndrome. Human Mutation. 38(4). 373–377. 17 indexed citations
13.
Shi, Lijun, Bryn D. Webb, Xiaoqiang Cai, et al.. (2016). Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease‐causing variants. Clinical Genetics. 91(4). 599–604. 17 indexed citations
14.
Webb, Bryn D., Patricia G. Wheeler, Jacob Hagen, et al.. (2015). Novel, Compound Heterozygous, Single-Nucleotide Variants inMARS2Associated with Developmental Delay, Poor Growth, and Sensorineural Hearing Loss. Human Mutation. 36(6). 587–592. 26 indexed citations
15.
Rucker, Janet C., Bryn D. Webb, Tamiesha Frempong, et al.. (2014). Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes. Brain. 137(4). 1068–1079. 12 indexed citations
16.
Webb, Bryn D., et al.. (2014). Evaluation of the Affymetrix CytoScan®Dx Assay for developmental delay. Expert Review of Molecular Diagnostics. 15(2). 185–192. 6 indexed citations
17.
Chew, Sheena, Ravikumar Balasubramanian, Wai‐Man Chan, et al.. (2013). A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3. Brain. 136(2). 522–535. 81 indexed citations
18.
Webb, Bryn D., Maru Barrera, Joseph Beyene, et al.. (2012). Determinants of quality of life in children with chronic somatic disease: pilot data from the GapS Questionnaire. Quality of Life Research. 22(2). 339–349. 4 indexed citations
19.
Webb, Bryn D., Sherin Shaaban, Harald Gaspar, et al.. (2012). HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice. The American Journal of Human Genetics. 91(1). 171–179. 53 indexed citations
20.
Crawford, Gregory E., Ingeborg Holt, James R. Whittle, et al.. (2005). Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS). Genome Research. 16(1). 123–131. 368 indexed citations

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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