MSX1 Variants is a genetic construct denoting specific allelic alterations in the MSX1 gene that are associated with disrupted odontogenesis and craniofacial development, particularly contributing to the etiology of non-syndromic cleft lip.
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2017–2026
7
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Publications
76
A Nonsense Mutation in MSX1 Causes Witkop Syndrome
Dolrudee Jumlongras, Marianna Bei, Jean M. Stimson et al. · The American Journal of Human Genetics · 2001 · 263 citations · Full text
Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate
Alexandre R. Vieira, Joseph R. Avila, Sandra Daack‐Hirsch et al. · PLoS Genetics · 2005 · 260 citations · Full text
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1–5 of 434
Institutions
181
University of Iowa
Iowa City, United States
11 h-index
60 publications
11.1K citations
Johns Hopkins University
Baltimore, United States
5 h-index
21 publications
1.9K citations
Aichi Gakuin University
Nagoya, Japan
5 h-index
26 publications
1.4K citations
Universidade Federal do Rio de Janeiro
Rio de Janeiro, Brazil
4 h-index
16 publications
2K citations
Poznan University of Medical Sciences
Poznan, Poland
4 h-index
12 publications
557 citations
University of Pittsburgh
Pittsburgh, United States
4 h-index
7 publications
1.1K citations
Johns Hopkins Medicine
Baltimore, United States
4 h-index
8 publications
742 citations
Aichi Human Service Center
Kasugai, Japan
3 h-index
18 publications
516 citations
1–8 of 181
Venues
- Journal of Dental Research
JDR · 7 publications · 665 citations
7
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- The Cleft Palate-Craniofacial Journal
5 publications · 282 citations
5
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- Archives of Oral Biology
4 publications · 143 citations
4
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- American Journal of Medical Genetics Part A
4 publications · 349 citations
4
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- European Journal Of Oral Sciences
4 publications · 117 citations
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