Claudio R. Cortés

Oakland University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index1.0kcitations19works0.02yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(8), Congenital heart defects research(5), Renal and related cancers(5), Hedgehog Signaling Pathway Studies(4), Microtubule and mitosis dynamics(3)

Publications19 total

Undergraduate medical students’ perceptions of an interactive and collaborative cloud-based learning strategy: survey at a single institution
BMC Medical Education·2026Open Access
Exploration of a Collaborative Self-Directed Learning Model in Medical Education
Medical Science Educator·2022· 67 citedOpen Access
Protocols for Investigating the Epithelial Properties of Cardiac Progenitor Cells in the Mouse Embryo
Methods in molecular biology·2022· 2 cited
EPySeg: a coding-free solution for automated segmentation of epithelia using deep learning
Development·2020· 52 citedOpen Access
Tbx1 regulates extracellular matrix-cell interactions in the second heart field
Human Molecular Genetics·2019· 36 citedOpen Access
T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field
Human Molecular Genetics·2018· 95 citedOpen Access
<i>Tbx1</i> regulates extracellular matrix-cell interactions in the second heart field
2018· 1 citedOpen Access
Epithelial Properties of the Second Heart Field
Circulation Research·2018· 54 citedOpen Access
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function
Scientific Reports·2016· 42 citedOpen Access
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function
QUT ePrints (Queensland University of Technology)·2016Open Access
Correction: Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
Nature Communications·2016· 259 citedOpen Access
Unmasking the ciliopathies: craniofacial defects and the primary cilium
Wiley Interdisciplinary Reviews Developmental Biology·2015· 42 cited
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
Nature Communications·2015· 81 citedOpen Access
Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy
The American Journal of Human Genetics·2013· 122 citedOpen Access
Short-rib polydactyly and jeune syndromes are caused by mutations in WDR60
QUT ePrints (Queensland University of Technology)·2013· 1 citedOpen Access
Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60
The American Journal of Human Genetics·2013· 131 citedOpen Access
Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy
QUT ePrints (Queensland University of Technology)·2013Open Access
Yeast-based assay identifies novel Shh/Gli target genes in vertebrate development
BMC Genomics·2012· 32 citedOpen Access
Sonic hedgehog (SHH) regulates c-myc expression in the developing brain: Direct or indirect link?
Developmental Biology·2009

Frequent Co-authors

Carol Wicking(8), Miriam Schmidts(6), Peter Scambler(6), Aideen McInerney‐Leo(6), Paul Leo(6), Matthew A. Brown(6), Andreas Zankl(6), Emma L. Duncan(6), Hannah M. Mitchison(5), Robert G. Kelly(5), Hülya Kayserili(4), Brooke Gardiner(4), Mhairi Marshall(4), Philip L. Beales(4), Jessica Harris(3), Christopher De Bono(3), Yuqing Hou(2), Dorus A. Mans(2), Céline Huber(2), Karsten Boldt(2)