Personal information

United States

Biography

Baylor College of Medicine, Houston, TX USA

Activities

Employment (1)

Baylor College of Medicine: Houston, TX, US

2022-02-01 to present | Assistant Professor (Molecular and Human Genetics)
Employment
Source: Self-asserted source
Kwanghyuk Lee

Works (41)

Evolutionary Action–Machine Learning Model Identifies Candidate Genes Associated With Early‐Onset Coronary Artery Disease

Journal of the American Heart Association
2023-09-05 | Journal article
Contributors: Dillon Shapiro; Kwanghyuk Lee; Jennifer Asmussen; Thomas Bourquard; Olivier Lichtarge
Source: check_circle
Crossref

Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease

Nature Communications
2023-05-13 | Journal article
Contributors: Thomas Bourquard; Kwanghyuk Lee; Ismael Al-Ramahi; Minh Pham; Dillon Shapiro; Yashwanth Lagisetty; Shirin Soleimani; Samantha Mota; Kevin Wilhelm; Maryam Samieinasab et al.
Source: check_circle
Crossref

Corrigendum to "The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition" [Behav. Brain Res. 223 (2011) 48-52]

Behavioural Brain Research
2013 | Journal article
DOI:

10.1016/j.bbr.2012.11.001

Contributors: Tomson, S.N.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease

American Journal of Human Genetics
2013 | Journal article
DOI:

10.1016/j.ajhg.2013.02.013

Contributors: Jenkinson, E.M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Proceedings of the National Academy of Sciences of the United States of America
2012 | Journal article
DOI:

10.1073/pnas.1120210109

Contributors: Celestino-Soper, P.B.S.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Alterations of the CIB2 calcium-and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

Nature Genetics
2012 | Journal article
DOI:

10.1038/ng.2426

Contributors: Riazuddin, S.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss

American Journal of Medical Genetics, Part A
2012 | Journal article
DOI:

10.1002/ajmg.a.34407

Contributors: Lee, K.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families

Clinical Genetics
2012 | Journal article
DOI:

10.1111/cge.12047

Contributors: Lee, K.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment

Clinical Genetics
2012 | Journal article
DOI:

10.1111/j.1399-0004.2011.01695.x

Contributors: Lee, K.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13

Journal of Human Genetics
2011 | Journal article
DOI:

10.1038/jhg.2011.110

Contributors: Ansar, M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia

Clinical Genetics
2011 | Journal article
DOI:

10.1111/j.1399-0004.2010.01529.x

Contributors: Mendoza-Fandino, G.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene

Archives of Otolaryngology - Head and Neck Surgery
2011 | Journal article
DOI:

10.1001/archoto.2010.234

Contributors: Arnett, J.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2

Human Genetics
2011 | Journal article
DOI:

10.1007/s00439-010-0934-0

Contributors: Basit, S.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74

American Journal of Human Genetics
2011 | Journal article
DOI:

10.1016/j.ajhg.2010.11.010

Contributors: Ahmed, Z.M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42

American Journal of Human Genetics
2011 | Journal article
DOI:

10.1016/j.ajhg.2010.12.011

Contributors: Borck, G.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

Human Genetics
2011 | Journal article
DOI:

10.1007/s00439-011-1018-5

Contributors: Rehman, A.U.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3

Human Heredity
2011 | Journal article
DOI:

10.1159/000320154

Contributors: Ali, G.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition

Behavioural Brain Research
2011 | Journal article
DOI:

10.1016/j.bbr.2011.03.071

Contributors: Tomson, S.N.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

American Journal of Human Genetics
2010 | Journal article
DOI:

10.1016/j.ajhg.2009.12.017

Contributors: Schraders, M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Terminal Osseous Dysplasia with Pigmentary Defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region

American Journal of Medical Genetics, Part A
2010 | Journal article
DOI:

10.1002/ajmg.a.33470

Contributors: Brunetti-Pierri, N.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome)

European Journal of Human Genetics
2009 | Journal article
DOI:

10.1038/ejhg.2008.255

Contributors: McBride, K.L.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32

Investigative Ophthalmology and Visual Science
2009 | Journal article
DOI:

10.1167/iovs.08-2173

Contributors: Gajecka, M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

American Journal of Human Genetics
2009 | Journal article
DOI:

10.1016/j.ajhg.2009.06.003

Contributors: Schultz, J.M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3

Journal of Human Genetics
2009 | Journal article
DOI:

10.1038/jhg.2009.2

Contributors: Chishti, M.S.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44 [4]

Clinical Genetics
2008 | Journal article
DOI:

10.1111/j.1399-0004.2008.00976.x

Contributors: Bhatti, A.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

American Journal of Human Genetics
2008 | Journal article
DOI:

10.1016/j.ajhg.2007.09.008

Contributors: Collin, R.W.J.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families

Journal of Human Genetics
2008 | Journal article
DOI:

10.1007/s10038-007-0209-3

Contributors: Chishti, M.S.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3

Human Genetics
2007 | Journal article
DOI:

10.1007/s00439-006-0246-6

Contributors: Mendoza, G.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2

Annals of Human Genetics
2007 | Journal article
DOI:

10.1111/j.1469-1809.2007.00362.x

Contributors: Wali, A.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan

Brain and Development
2006 | Journal article
DOI:

10.1016/j.braindev.2005.11.003

Contributors: El-Shanti, H.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type

Journal of Medical Genetics
2006 | Journal article
DOI:

10.1136/jmg.2005.033381

Contributors: Naeem, M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3

Human Genetics
2006 | Journal article
DOI:

10.1007/s00439-005-0079-8

Contributors: Hassan, M.J.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2

Human Genetics
2006 | Journal article
DOI:

10.1007/s00439-006-0188-z

Contributors: Santos, R.L.P.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

Ectodermal dysplasia of hair and nail type: Mapping of a novel locus to chromosome 17p12-q21.2

British Journal of Dermatology
2006 | Journal article
DOI:

10.1111/j.1365-2133.2006.07509.x

Contributors: Naeem, M.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32

Journal of Molecular Medicine
2006 | Journal article
DOI:

10.1007/s00109-005-0023-3

Contributors: Tariq, A.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier
grade
Preferred source (of 2)‎

Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment

Journal of Molecular Medicine
2006 | Journal article
DOI:

10.1007/s00109-005-0015-3

Contributors: Santos, R.L.P.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23

Clinical Genetics
2006 | Journal article
DOI:

10.1111/j.1399-0004.2006.00611.x

Contributors: Ali, G.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2

Clinical Genetics
2005 | Journal article
DOI:

10.1111/j.1399-0004.2005.00492.x

Contributors: Irshad, S.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.

Human mutation.
2005 | Journal article
Contributors: Santos, R.L.
Source: Self-asserted source
Kwanghyuk Lee via Scopus - Elsevier

The genetics of colored sequence synesthesia: Evidence of linkage to chromosome 16q and genetic heterogeneity for the condition

Journal article
DOI:

http://dx.doi.org/10.1038/npre.2009.3987.1

Source: Self-asserted source
Kwanghyuk Lee

The genetics of colored sequence synesthesia: Evidence of linkage to chromosome 16q and genetic heterogeneity for the condition

Journal article
DOI:

http://dx.doi.org/10.1038/npre.2009.3987

Source: Self-asserted source
Kwanghyuk Lee