Richard A. Gibbs

ScholarGPS® ID: 12916028616018

Affiliation
Baylor College of Medicine, Houston, United States
Affiliation History

Field
Life Sciences
Discipline
Genetics
Top Specialties
Mutation | Genomics | Exome Sequencing | DNA | Human Genetics | Medical Genetics | Cancer | Molecular Genetics | DNA Sequencing | Whole Genome Sequencing | Polymerase Chain Reaction | Chain Reaction | Birth Defect | Neoplasm | Chromosome
Metrics Summary
Publication Count
510
Predicted Citations
47,617
Predicted h-index
113
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
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Empowering personalized pharmacogenomics with generative AI solutions (journal article)
Murugan, Mullai | Yuan, Bo | Venner, Eric | Ballantyne, Christie M | Robinson, Katherine M | Coons, James C | Wang, Liwen | Empey, Philip E | Gibbs, Richard A
Journal of the American Medical Informatics Association, volume 31, issue 6, pages 1356-1366 (2024).
10.1093/jamia/ocae039
Cited by (4) | Cite | Source
Validation of Single‐Nucleotide Mosaic Variants Through Droplet Digital PCR (journal article)
Grochowski, Christopher M. | Gibbs, Richard A. | Doddapaneni, Harsha
Current Protocols, volume 4, issue 5 (2024).
10.1002/cpz1.1041
Cite | Source
Somatic mutations of esophageal adenocarcinoma: a comparison between Black and White patients (journal article)
Lim, Hyeyeun | Gingras, Marie-Claude | Zhao, Jing | Byun, Jinyoung | Castro, Patricia D. | Tsavachidis, Spiridon | Hu, Jianhong | Doddapaneni, Harshavardhan | Han, Yi | Muzny, Donna M. | ... | Thrift, Aaron P.
Scientific Reports, volume 14, issue 1 (2024).
10.1038/s41598-024-59257-3
Cite | Source
Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders (journal article)
Bozkurt-Yozgatli, Tugce | Pehlivan, Davut | Gibbs, Richard A. | Sezerman, Ugur | Posey, Jennifer E. | Lupski, James R. | Coban-Akdemir, Zeynep
BMC Medical Genomics, volume 17, issue 1 (2024).
10.1186/s12920-024-01852-4
Cite | Source
NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy (journal article)
Dardas, Zain | Fatih, Jawid M. | Jolly, Angad | Dawood, Moez | Du, Haowei | Grochowski, Christopher M. | Jones, Edward G. | Jhangiani, Shalini N. | Wehrens, Xander H. T. | Liu, Pengfei | ... | Morris, Shaine A.
Genome Medicine, volume 16, issue 1 (2024).
10.1186/s13073-024-01312-9
Cite | Source
O01: Using multiplexed functional data to reduce the VUS burden in populations underrepresented in genomic medicine (journal article)
Dawood, Moez | Fayer, Shawn | Post, Mason | Kalra, Divya | Patterson, Karynne | Venner, Eric | Muffley, Lara | Fowler, Douglas | Rubin, Alan | Gibbs, Richard | ... | Romero, Irene Gallego
Genetics in Medicine Open, volume 2 (2024).
10.1016/j.gimo.2024.101010
Cite | Source
Novel LSS variants in alopecia and intellectual disability syndrome: New case report and clinical spectrum of LSS ‐related rare disease traits (journal article)
Elbendary, Hasnaa M. | Marafi, Dana | Saad, Ahmed K. | Elhossini, Rasha | Duan, Ruizhi | Rafat, Karima | Jhangiani, Shalini N. | Gibbs, Richard A. | Pehlivan, Davut | Calame, Daniel G. | ... | Zaki, Maha S.
Clinical Genetics, volume 104, issue 3, pages 344-349 (2023).
10.1111/cge.14348
Cited by (1) | Cite | Source
Precision Neurology for Dementia (P2-6.002) (journal article)
Shulman, Joshua | Vanegas-Arroyave, Nora | Fong, Jamie | Elsea, Sarah | Lin, Chi-ing | Saade, Hiba | Chavez, Fatima | Walker, Kimberly | Yuan, Bo | Venner, Eric | ... | Masdeu, Joseph
Neurology, volume 100, issue 17_supplement_2 (2023).
10.1212/WNL.0000000000203706
Cited by (1) | Cite | Source
Modeling nonsegmented negative-strand RNA virus (NNSV) transcription with ejective polymerase collisions and biased diffusion (journal article)
Piedra, Felipe-Andrés | Henke, David | Rajan, Anubama | Muzny, Donna M. | Doddapaneni, Harsha | Menon, Vipin K. | Hoffman, Kristi L. | Ross, Matthew C. | Javornik Cregeen, Sara J. | Metcalf, Ginger | ... | Piedra, Pedro A.
Frontiers in Molecular Biosciences, volume 9 (2023).
10.3389/fmolb.2022.1095193
Cited by (1) | Cite | Source
xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments (journal article)
Farek, Jesse | Hughes, Daniel | Salerno, William | Zhu, Yiming | Pisupati, Aishwarya | Mansfield, Adam | Krasheninina, Olga | English, Adam C | Metcalf, Ginger | Boerwinkle, Eric | ... | Sedlazeck, Fritz J
GigaScience, volume 12 (2022).
10.1093/gigascience/giac125
Cited by (8) | Cite | Source
Truvari: refined structural variant comparison preserves allelic diversity (journal article)
English, Adam C. | Menon, Vipin K. | Gibbs, Richard A. | Metcalf, Ginger A. | Sedlazeck, Fritz J.
Genome Biology, volume 23, issue 1 (2022).
10.1186/s13059-022-02840-6
Cited by (50) | Cite | Source
Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study (journal article)
Smith, Hadley Stevens | Sanchez, Clarissa E. | Maag, Ronald | Buentello, Alexandria | Murdock, David R. | Metcalf, Ginger A. | Hadley, Trevor D. | Riconda, Daniel L. | Boerwinkle, Eric | Wehrens, Xander H.T. | ... | Pereira, Stacey
Circulation: Genomic and Precision Medicine, volume 15, issue 6 (2022).
10.1161/CIRCGEN.121.003605
Cite | Source
Clinical and molecular features of pediatric cancer patients with Lynch syndrome (journal article)
Scollon, Sarah | Eldomery, Mohammad K. | Reuther, Jacquelyn | Lin, Frank Y. | Potter, Samara L. | Desrosiers, Lauren | McClain, Kenneth L. | Smith, Valeria | Su, Jack Meng‐Fen | Venkatramani, Rajkumar | ... | Plon, Sharon E.
Pediatric Blood & Cancer, volume 69, issue 11 (2022).
10.1002/pbc.29859
Cited by (8) | Cite | Source
Harmonizing variant classification for return of results in the All of Us Research Program (journal article)
Harrison, Steven M. | Austin‐Tse, Christina A. | Kim, Serra | Lebo, Matthew | Leon, Annette | Murdock, David | Radhakrishnan, Aparna | Shirts, Brian H. | Steeves, Marcie | Venner, Eric | ... | Rehm, Heidi L.
Human Mutation, volume 43, issue 8, pages 1114-1121 (2022).
10.1002/humu.24317
Cited by (7) | Cite | Source
C. Thomas Caskey, M.D. (1938–2022): A remembrance (journal article)
Beaudet, Arthur L. | Gibbs, Richard A.
The American Journal of Human Genetics, volume 109, issue 7, pages 1185-1189 (2022).
10.1016/j.ajhg.2022.05.012
Cite | Source
Novel RETREG1 ( FAM134B) founder allele is linked to HSAN2B and renal disease in a Turkish family (journal article)
Taşdelen, Elifcan | Calame, Daniel G. | Akay, Gulsen | Mitani, Tadahiro | Fatih, Jawid M. | Herman, Isabella | Du, Haowei | Coban‐Akdemir, Zeynep | Marafi, Dana | Jhangiani, Shalini N. | ... | Pehlivan, Davut
American Journal of Medical Genetics Part A, volume 188, issue 7, pages 2153-2161 (2022).
10.1002/ajmg.a.62727
Cited by (4) | Cite | Source
Multiple Respiratory Syncytial Virus (RSV) Strains Infecting HEp-2 and A549 Cells Reveal Cell Line-Dependent Differences in Resistance to RSV Infection (journal article)
Rajan, Anubama | Piedra, Felipe-Andrés | Aideyan, Letisha | McBride, Trevor | Robertson, Matthew | Johnson, Hannah L. | Aloisio, Gina Marie | Henke, David | Coarfa, Cristian | Stossi, Fabio | ... | Piedra, Pedro A.
Journal of Virology, volume 96, issue 7 (2022).
10.1128/jvi.01904-21
Cited by (13) | Cite | Source
Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome (journal article)
Garcia, Annie | Desrosiers, Lauren | Scollon, Sarah | Gruner, Stephanie | Reuther, Jacquelyn | Gandhi, Ilavarasi | Patil, Ninad | Fuller, Maren Y. | Dai, Hongzheng | Muzny, Donna | ... | Roy, Angshumoy
Cancer Genetics, volume 262-263 (2022).
10.1016/j.cancergen.2022.01.001
Cited by (2) | Cite | Source
Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses (journal article)
Herman, Isabella | Jolly, Angad | Du, Haowei | Dawood, Moez | Abdel‐Salam, Ghada M. H. | Marafi, Dana | Mitani, Tadahiro | Calame, Daniel G. | Coban‐Akdemir, Zeynep | Fatih, Jawid M. | ... | Lupski, James R.
American Journal of Medical Genetics Part A, volume 188, issue 3, pages 735-750 (2022).
10.1002/ajmg.a.62565
Cited by (13) | Cite | Source
C. Thomas Caskey (1938–2022) (journal article)
Gibbs, Richard A. | Chakravarti, Aravinda | Eichler, Evan E. | Green, Eric D. | Myers, Richard M. | Ferguson-Smith, Anne C. | Makova, Kateryna D. | Sussman, Hillary E.
Genome Research, volume 32, issue 3, pages vii-viii (2022).
10.1101/gr.276658.122
Cited by (1) | Cite | Source