Byron L. Lam

Dr. Byron L. Lam

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2019 in American Journal of Ophthalmology
Verified
Journal Article
Closed access
BLByron L. Lam
Byron L. Lam
JDJanet L. Davis
Janet L. Davis
NGNinel Z. Gregori
Ninel Z. Gregori
RMRobert E MacLaren
Robert E MacLaren
AGAniz Girach
Aniz Girach
WFWilliam J. Feuer
William J. Feuer

1 February 2011 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
SZStephan Züchner
Stephan Züchner
JDJulia Dallman
Julia Dallman
RWRong Wen
Rong Wen
GBGary Beecham
Gary Beecham
ANAdam Naj
Adam Naj
MPMargaret A. Pericak-Vance
Margaret A. Pericak-Vance

1 June 2010 in Ophthalmology
Verified
Journal Article
Closed access
SWSaloni Walia
Saloni Walia
GFGerald A. Fishman
Gerald A. Fishman
SJSamuel Jacobson
Samuel Jacobson
TATomas S. Aleman
Tomas S. Aleman
RKRobert Koenekoop
Robert Koenekoop
ESEdwin M. Stone
Edwin M. Stone

1 September 2008 in Current Neurology and Neuroscience Reports
Verified
Journal Article
Closed access
PDF file
BLByron L. Lam
Byron L. Lam
CMChristopher G. Morais
Christopher G. Morais
JPJoshua Pasol
Joshua Pasol

1 April 2014 in JAMA Ophthalmology
Verified
Journal Article
Closed access
PDF file
BLByron L. Lam
Byron L. Lam
WFWilliam J. Feuer
William J. Feuer
JSJoyce C. Schiffman
Joyce C. Schiffman
VPVittorio Porciatti
Vittorio Porciatti
RVRuth Vandenbroucke
Ruth Vandenbroucke
JGJohn Guy
John Guy
Research from JAMA Ophthalmology — Trial End Points and Natural History in Patients With G11778A Leber Hereditary Optic Neuropathy — Preparation for Gene Therapy Clinical Trial

14 December 2021 in Orphanet Journal of Rare Diseases
Verified
Journal Article
Open access
PDF file
BLByron L. Lam
Byron L. Lam
BLBart P. Leroy
Bart P. Leroy
GBGraeme Black
Graeme Black
TOTuyen Ong
Tuyen Ong
DYDan Yoon
Dan Yoon
KTKarmen Trzupek
Karmen Trzupek
Inherited retinal diseases (IRDs) are a diverse group of degenerative diseases of the retina that can lead to significant reduction in vision and blindness. Because of the considerable phenotypic overlap among IRDs, genetic testing is a critical step in obtaining a definitive diagnosis for affected individuals and enabling access to emerging gene therapy–based treatments and ongoing clinical studies. While advances in molecular diagnostic technologies have significantly improved the understanding of IRDs and identification of disease-causing variants, training in genetic diagnostics among ophthalmologists is limited. In this review, we will provide ophthalmologists with an overview of genetic testing for IRDs, including the types of available testing, variant interpretation, and genetic counseling. Additionally, we will discuss the clinical applications of genetic testing in the molecular diagnosis of IRDs through case studies.