Rick A. Martin

Washington University in St. Louis — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

24h-index2.3kcitations43works0.02yr avg
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Research Topics

Craniofacial Disorders and Treatments(8), Cleft Lip and Palate Research(7), Prenatal Screening and Diagnostics(6), Genetic Syndromes and Imprinting(6), Lysosomal Storage Disorders Research(5)

Publications43 total

Residential greenness and cardiovascular disease incidence, readmission, and mortality
ISEE Conference Abstracts·2020· 2 citedOpen Access
GPC3 and the Simpson-Golabi-Behmel Syndrome
Oxford University Press eBooks·2016
The importance of mentors in a 20‐year gestation
American Journal of Medical Genetics Part A·2010
Novel Cleft Susceptibility Genes in Chromosome 6q
Journal of Dental Research·2010· 32 cited
Four-Year Prospective Clinical Trial of Agalsidase Alfa in Children with Fabry Disease
The Journal of Pediatrics·2010· 57 cited
Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate
American Journal of Medical Genetics Part A·2009· 39 citedOpen Access
Multidisciplinary Management of Hunter Syndrome
PEDIATRICS·2009· 192 cited
Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia
Genetics in Medicine·2009· 95 citedOpen Access
AXIS inhibition protein 2, orofacial clefts and a family history of cancer
The Journal of the American Dental Association·2009· 91 cited
Eighth International Symposium on Lysosomal Storage Diseases.
PubMed·2009
Am J Med Genet Part A 146A:1101–1116 Development and validation of a measure of dysmorphology: Useful for autism subgroup classification
American Journal of Medical Genetics Part A·2008· 3 cited
<i>GPC3 </i>and the Simpson–Golabi–Behmel Syndrome
2008
Development and validation of a measure of dysmorphology: Useful for autism subgroup classification
American Journal of Medical Genetics Part A·2008· 72 cited
29 Clinical benefit of enzyme replacement therapy (ERT) in mucopolysaccharidosis II (MPS II, Hunter syndrome)
Molecular Genetics and Metabolism·2007· 2 cited
Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate
American Journal of Medical Genetics Part A·2007· 84 cited
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
Genetics in Medicine·2006· 269 citedOpen Access
Anthropometric Precision and Accuracy of Digital Three-Dimensional Photogrammetry
Journal of Craniofacial Surgery·2006· 338 cited
The Pittsburgh Oral-Facial Cleft Study: Expanding the Cleft Phenotype. Background and Justification
The Cleft Palate-Craniofacial Journal·2006· 110 cited
Say what we mean, mean what we say
European Journal of Human Genetics·2005Open Access
Male Genital System
2005
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Frequent Co-authors

Mary L. Marazita(6), Seth M. Weinberg(4), M. Anne Spence(4), Christine M. Eng(3), Katherine Neiswanger(3), Margaret E. Cooper(3), Kathleen M. Bardi(3), Carla A. Brandon(3), Alexandre R. Vieira(3), Kenneth Lyons Jones(3), Kenneth L. Jones(3), Kurt Benirschke(3), Michael R. DeBaun(3), Alex A. Kane(2), Joseph Muenzer(2), Michael Beck(2), Roberto Giugliani(2), Paul Harmatz(2), Christoph Kampmann(2), Uma Ramaswami(2)