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Genetics

D-Index
105
Citations
35776
World Ranking
630
National Ranking
318

Medicine

D-Index
112
Citations
42188
World Ranking
5181
National Ranking
2801

Overview

Richard A. Lewis is a researcher affiliated with Baylor College of Medicine in the United States. Their work spans a range of topics primarily within biochemistry, genetics, molecular biology, and medicine, with a significant focus on genetics and molecular biology research.

The research conducted by Richard A. Lewis covers various subfields including genetics, molecular biology, ophthalmology, neurology, and radiology, nuclear medicine, and imaging. Their investigations address multiple medical and biological topics such as glaucoma and retinal disorders, retinal diseases and treatments, genomics and rare diseases, genomic variations and chromosomal abnormalities, genetics and neurodevelopmental disorders, congenital heart defects research, and ocular surface and contact lens studies.

Frequent co-authors in their research collaborations include Jill A. Rosenfeld, Carlos A. Bacino, Lindsay C. Burrage, Brendan Lee, and Alyssa A. Tran, reflecting ongoing scientific partnerships across multiple projects.

Their research outputs are often published in established venues, including:

  • American Journal of Medical Genetics Part A
  • The American Journal of Human Genetics
  • arXiv (Cornell University)
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Molecular Genetics & Genomic Medicine

Recent publications by Richard A. Lewis include:

  • Long-term Outcomes of Adding Lutein/Zeaxanthin and ω-3 Fatty Acids to the AREDS Supplements on Age-Related Macular Degeneration Progression, 2022, JAMA Ophthalmology
  • Fixed-Dose Combination of Netarsudil and Latanoprost in Ocular Hypertension and Open-Angle Glaucoma: Pooled Efficacy/Safety Analysis of Phase 3 MERCURY-1 and -2, 2020, Advances in Therapy
  • Pooled Efficacy and Safety Profile of Netarsudil Ophthalmic Solution 0.02% in Patients With Open-angle Glaucoma or Ocular Hypertension, 2020, Journal of Glaucoma
  • Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science, 2020, Genetics in Medicine
  • Four-Year Outcomes of Two Second-Generation Trabecular Micro-Bypass Stents in Patients with Open-Angle Glaucoma on One Medication, 2020, Clinical Ophthalmology

Best Publications

  • A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

    Rando Allikmets;Nanda Singh;Hui Sun;Noah F. Shroyer

  • Mutations in smooth muscle α-actin ( ACTA2 ) lead to thoracic aortic aneurysms and dissections

    Dong Chuan Guo;Hariyadarshi Pannu;Van Tran-Fadulu;Christina L. Papke

  • Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.

    Asmae Smahi;G. Courtois;P. Vabres;S. Yamaoka

  • Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome

    Stephen J. Ansley;Jose L. Badano;Oliver E. Blacque;Josephine Hill

  • Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder

    Nicholas Katsanis;Stephen J. Ansley;Jose L. Badano;Erica R. Eichers

  • Multifocal demyelinating neuropathy with persistent conduction block

    Richard A. Lewis;Austin J. Sumner;Mark J. Brown;Arthur K. Asbury

  • The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.

    Attree O;Olivos Im;Okabe I;Bailey Lc

  • Neurological dysfunction and axonal degeneration in Charcot–Marie–Tooth disease type 1A

    Karen M. Krajewski;Richard A. Lewis;Darren R. Fuerst;Cheryl Turansky

  • Reliability and validity of the CMT neuropathy score as a measure of disability

    Michael E. Shy;J. Blake;K. Krajewski;D. R. Fuerst

  • Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome

    Carmen C Leitch;Norann A Zaghloul;Erica E Davis;Corinne Stoetzel

  • Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.

    Lorraine Potocki;Weimin Bi;Diane Treadwell-Deering;Claudia M. B. Carvalho

  • Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

    Frank Greenberg;Richard A. Lewis;Lorraine Potocki;Daniel Glaze

  • Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling

    Moumita Chaki;Rannar Airik;Amiya K. Ghosh;Rachel H. Giles

  • Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.

    Bassem A. Bejjani;Richard Alan Lewis;Karim F. Tomey;Kent L. Anderson

  • Practice Parameter: Evaluation of distal symmetric polyneuropathy: Role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review) Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation

    J. D. England;J. D. England;G. S. Gronseth;G. Franklin;G. T. Carter

  • Molecular Genetics of Human Blue Cone Monochromacy

    Jeremy Nathans;Carol M. Davenport;Irene H. Maumenee;Richard Alan Lewis

  • TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

    Erica E. Davis;Qi Zhang;Qin Liu;Bill H. Diplas

  • von Recklinghausen neurofibromatosis. II. Incidence of optic gliomata.

    Lewis Ra;Gerson Lp;Axelson Ka;Riccardi Vm

  • Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

    Edgar A Otto;Toby W Hurd;Rannar Airik;Moumita Chaki

  • Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder.

    N Katsanis;SJ Ansley;JL Badano;ER Eichers

Frequent Co-Authors

James R. Lupski
James R. Lupski Baylor College of Medicine
Nicholas Katsanis
Nicholas Katsanis Galatea Bio Inc
Richard A. Gibbs
Richard A. Gibbs Baylor College of Medicine
Philip L. Beales
Philip L. Beales University College London
Donna M. Muzny
Donna M. Muzny Baylor College of Medicine
Lorraine Potocki
Lorraine Potocki Baylor College of Medicine
Erica E. Davis
Erica E. Davis Lurie Children's Hospital
Christian P. Schaaf
Christian P. Schaaf Baylor College of Medicine
Robert L. Nussbaum
Robert L. Nussbaum University of California, San Francisco
David L. Nelson
David L. Nelson Baylor College of Medicine

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