Nancy J. Carpenter

University of Wisconsin–La Crosse — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

31h-index4.0kcitations108works3.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(44), Genomic variations and chromosomal abnormalities(25), Autism Spectrum Disorder Research(16), Prenatal Screening and Diagnostics(12), Congenital heart defects research(10)

Publications108 total

The impact of topical capsaicin application on the muscle metaboreflex and microvascular responsiveness
Physiological Reports·2025Open Access
A randomized, double-blinded, phase 2 trial of EDP1815, an oral immunomodulatory preparation of Prevotella histicola, in adults with mild-to-moderate plaque psoriasis
Frontiers in Medicine·2024· 6 citedOpen Access
Clinical translation of anti-inflammatory effects of Prevotella histicola in Th1, Th2, and Th17 inflammation
Frontiers in Medicine·2023· 16 citedOpen Access
Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population
UNC Libraries·2020Open Access
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies
UNC Libraries·2020· 25 citedOpen Access
Forward and inverse methods for extracting climate and diet information from stable isotope profiles in proboscidean molars
Quaternary International·2020· 26 cited
Molecular Genetics and Diagnostic Testing
2019
Microdeletion Syndromes
2019
Le grand bateau de grand ours
2014
Developmental Trajectories in Syndromes With Intellectual Disability, With a Focus on Wolf-Hirschhorn and Its Cognitive–Behavioral Profile
American Journal on Intellectual and Developmental Disabilities·2012· 29 cited
Der kleine Bär und sein kleines Boot
Medical Entomology and Zoology·2011
The course of cognitive‐behavioral development in children with the <i>FMR1</i> mutation, Williams–Beuren syndrome, and neurofibromatosis type 1: The effect of gender
American Journal of Medical Genetics Part A·2010· 29 cited
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies
Proceedings of the National Academy of Sciences·2009· 393 citedOpen Access
Developmental Disabilities
2008
Studies of age‐correlated features of cognitive‐behavioral development in children and adolescents with genetic disorders
American Journal of Medical Genetics Part A·2007· 50 cited
Developmental Disabilities
2007
Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation
The American Journal of Human Genetics·2006· 122 citedOpen Access
Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
The American Journal of Human Genetics·2005· 366 citedOpen Access
Molecular Genetics and Diagnostic Testing
2005
Microdeletion Syndromes
2005
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Frequent Co-authors

Jeanette J. A. Holden(9), Patricia N. Howard‐Peebles(9), Gene S. Fisch(8), Burhan Say(8), Richard J. Simensen(7), Charles E. Schwartz(5), Anne Maddalena(5), Jack Tarleton(4), H Veenema(3), P. Pearson(3), Walter E. Nance(3), Julie R. Korenberg(2), Arthur S. Aylsworth(2), Barbara McGillivray(2), John B. Moeschler(2), Roger E. Stevenson(2), Virginia K. Proud(2), Huw Dorkins(2), Gillian Turner(2), Marten H. Hofker(2)