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Cell Reports|July 13, 2022
Single-cell atlas of craniogenesis uncovers SOXC-dependent, highly proliferative, and myofibroblast-like osteodermal progenitorsMarco Angelozzi, Renata Pellegrino da Silva, Michael V Gonzalez, et al.
Journal of Assisted Reproduction and Genetics|November 7, 2016
Copy number variation analysis reveals additional variants contributing to endometriosis developmentFernanda Mafra, Diego Mazzotti, Renata Pellegrino, et al.
BMC Genomics|June 1, 2013
Sleep is not just for the brain: transcriptional responses to sleep in peripheral tissuesRon C Anafi, Renata Pellegrino, Keith R Shockley, et al.
Genes|December 23, 2022
Association of Inherited Copy Number Variation in <i>ADAM3A</i> and <i>ADAM5</i> Pseudogenes with Oropharynx Cancer Risk and OutcomeJuliana Carron, Caroline Torricelli, Janet Keller Silva, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twinsTara Wenger, Dong Li, Margaret H Harr, et al.
Sleep|March 2, 2011
Effects of the adenosine deaminase polymorphism and caffeine intake on sleep parameters in a large population sampleDiego Robles Mazzotti, Camila Guindalini, Renata Pellegrino, et al.
Clinical Oral Investigations|September 9, 2021
Effect of micro-osteoperforations on the gene expression profile of the periodontal ligament of orthodontically moved human teethAlice Spitz, Daniel Adesse, Michael Gonzalez, et al.
Journal of Medical Case Reports|September 11, 2012
Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case reportRoberta S Guilherme, Vera de Fa Meloni, Sylvia S Takeno, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2016
A current snapshot of common genomic variants contribution in psychiatric disordersMarcos L Santoro, Patricia N Moretti, Renata Pellegrino, et al.
The Journal of Clinical Endocrinology and Metabolism|March 8, 2014
Genome-wide copy number analysis in a family with p.G533C RET mutation and medullary thyroid carcinoma identified regions potentially associated with a higher predisposition to lymph node metastasisAline N Araujo, Lais Moraes, Maria Inez C França, et al.
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