L. Wong

Baylor College of Medicine — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index1.6kcitations43works0.02yr avg
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Research Topics

Mitochondrial Function and Pathology(8), Alzheimer's disease research and treatments(6), RNA Research and Splicing(6), Metabolism and Genetic Disorders(6), Genomics and Chromatin Dynamics(5)

Publications42 total

Congenital muscular dystrophy in Taiwan: a referral center experience
Neuromuscular Disorders·2017· 1 cited
Next-Generation Sequencing Based Testing for Disorders of the Skeleton
2017
Crystal structure of pathogenic mutants of human mitochodnrial PheRS
2016
Safety and efficacy of rapid (1,000 mg in 1 hr) intravenous iron dextran for treatment of maternal iron deficient anemia of pregnancy
American Journal of Hematology·2016· 50 cited
Altered gene expression in <i>Henmt1</i><sup><i>PIN/PIN</i></sup> spermatocytes and round spermatids.
Figshare·2015Open Access
Next-generation sequencing for disorders of low and high bone mineral density
Osteoporosis International·2013· 58 citedOpen Access
Mitochondrial DNA polymerase γ mutations: an ever expanding molecular and clinical spectrum
Journal of Medical Genetics·2011· 155 cited
An new mutation m.3928G>C p.V208L in ND1 causes Leigh disease
Mitochondrion·2011
Proliferative and migratory aptitude in pterygium
Histochemistry and Cell Biology·2010· 36 cited
64 Mitochondrial depletion syndrome associated with pyruvate dehydrogenase deficiency
Mitochondrion·2010
05-P009 Role of replacement histone H3.3 in mammalian germ cell development
Mechanisms of Development·2009
Finding <i>twinkle</i> in the eyes of a 71‐year‐old lady: A case report and review of the genotypic and phenotypic spectrum of <i>TWINKLE</i>‐related dominant disease
American Journal of Medical Genetics Part A·2009· 56 cited
Patterns of Genetic Variation in the Hypertension Candidate Gene <i>GRK4</i>: Ethnic Variation and Haplotype Structure
Annals of Human Genetics·2005· 47 cited
312 IS THE VARIABLE CLINICAL PHENOTYPE ASSOCIATED WITH THE T8993G NARP (NEUROPATHY, ATAXIA, RETINITIS PIGMENTOSA) MITOCHONDRIAL DNA MUTATION SOLELY A FUNCTION OF DEGREE OF HETEROPLASMY?
Journal of Investigative Medicine·2004
Design and Use of a Peptide Nucleic Acid for the Detection of the Heteroplasmic Low-Frequency Melas Mutation in Human Mitochondrial DNA
Environmental and Molecular Mutagenesis·2002
Hereditary nonpolyposis colorectal cancer with gynecologic malignancies: report of two families in Taiwan.
PubMed·2001· 7 cited
Novel nucleotide substitutions in mitochondrial DNA
Journal of Inherited Metabolic Disease·1998· 1 cited
Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene
Human Genetics·1998· 12 cited
Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease
European Journal of Pediatrics·1998· 74 cited
Cystic fibrosis in a Puerto Rican female homozygous for the R1066C mutation.
Journal of Medical Genetics·1998· 13 citedOpen Access
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Frequent Co-authors

D. R. Crapper McLachlan(12), Walter J. Lukiw(9), C. Bergeron(5), May Kung Sutherland(5), Martin J. Somerville(4), Patricia Handley(3), Shan S. Wong(3), Min‐Hui Liang(3), Sandesh C.S. Nagamani(2), C. Rice(2), Е. И. Рогаев(2), Peter St George‐Hyslop(2), Larry K.K. Yoong(2), Craig A. Mizzen(2), M. E. Percy(2), Darren G. Monckton(1), Tetsuo Ashizawa(1), C. Thomas Caskey(1), Sha Tang(1), Jing Wang(1)