Renata Pellegrino

Renata Pellegrino

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Renata Pellegrino

Renata Pellegrino

Publications by authors named "Renata Pellegrino"

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35Publications

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DGCR2 influences cortical thickness through a mechanism independent of schizophrenia pathogenesis.

Psychiatry Res 2019 04 27;274:391-394. Epub 2019 Feb 27.

Laboratório Interdisciplinar de Neurociências Clínicas (LiNC), Departamento de Psiquiatria, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil; Departamento de Psiquiatria, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.

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http://dx.doi.org/10.1016/j.psychres.2019.02.068DOI Listing
April 2019

Effects of the interaction between genetic factors and maltreatment on child and adolescent psychiatric disorders.

Psychiatry Res 2019 03 29;273:575-577. Epub 2019 Jan 29.

Genetics Division of the Department of Morphology and Genetics, Universidade Federal de São Paulo (UNIFESP), Brazil; Interdisciplinary Laboratory of Clinical Neurosciences (LiNC), UNIFESP, Brazil; Department of Psychiatry, UNIFESP, Brazil. Electronic address:

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http://dx.doi.org/10.1016/j.psychres.2019.01.078DOI Listing
March 2019

Implications of an admixed Brazilian population in schizophrenia polygenic risk score.

Schizophr Res 2019 Feb 26;204:404-406. Epub 2018 Jul 26.

Departamento de Morfologia e Genética da Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil; Laboratório Interdisciplinar de Neurociências Clínicas (LiNC) do Departamento de Psiquiatria da UNIFESP, São Paulo, Brazil; Departamento de Psiquiatria da UNIFESP, São Paulo, Brazil. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S09209964183047
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http://dx.doi.org/10.1016/j.schres.2018.07.026DOI Listing
February 2019

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

J Pediatr 2018 03 18;194:248-252.e2. Epub 2017 Dec 18.

Section of Dermatology, Department of Pediatrics, The Children's Hospital of Philadelphia and University of Pennsylvania Perlman School of Medicine, Philadelphia, PA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00223476173150
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http://dx.doi.org/10.1016/j.jpeds.2017.11.011DOI Listing
March 2018

Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins.

Am J Med Genet A 2018 01 12;176(1):75-81. Epub 2017 Nov 12.

Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.a.38516DOI Listing
January 2018

Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy.

Hum Mutat 2017 05 10;38(5):507-510. Epub 2017 Mar 10.

The Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/humu.23188DOI Listing
May 2017

Copy number variation analysis reveals additional variants contributing to endometriosis development.

J Assist Reprod Genet 2017 Jan 5;34(1):117-124. Epub 2016 Nov 5.

Collective Health Department, Division of Sexual and Reproductive Health Care and Population Genetics, Faculdade de Medicina do ABC, Santo André, SP, Brazil.

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http://dx.doi.org/10.1007/s10815-016-0822-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330977PMC
January 2017

A current snapshot of common genomic variants contribution in psychiatric disorders.

Am J Med Genet B Neuropsychiatr Genet 2016 12 3;171(8):997-1005. Epub 2016 Aug 3.

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.b.32475DOI Listing
December 2016

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.

J Immunol 2015 Aug 17;195(4):1599-607. Epub 2015 Jul 17.

Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, PA 19104; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104

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http://dx.doi.org/10.4049/jimmunol.1402310DOI Listing
August 2015

CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations.

Sci Rep 2015 Aug 21;5:13391. Epub 2015 Aug 21.

Center for Applied Genomics, Abramson Research Center, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1038/srep13391DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543987PMC
August 2015

Gene expression in B-1 cells from lupus-prone mice.

Immunol Invest 2014 20;43(7):675-92. Epub 2014 Jun 20.

Disciplina de Imunologia, Departamento de Microbiologia, Imunologia e Parasitologia Universidade Federal de São Paulo , Brazil .

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http://dx.doi.org/10.3109/08820139.2014.915413DOI Listing
May 2015

A novel BHLHE41 variant is associated with short sleep and resistance to sleep deprivation in humans.

Sleep 2014 Aug 1;37(8):1327-36. Epub 2014 Aug 1.

Center for Sleep and Circadian Neurobiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA ; Division of Sleep Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

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http://dx.doi.org/10.5665/sleep.3924DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096202PMC
August 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 metastasis.

J Clin Endocrinol Metab 2014 Jun 6;99(6):E1104-12. Epub 2014 Mar 6.

Genetic Bases of Thyroid Tumors Laboratory (A.N.A., L.M., J.M.C.), Division of Genetics, Department of Morphology and Genetics, Universidade Federal de São Paulo, and Laboratory of Molecular and Translational Endocrinology (M.I.C.F., R.M.B.M.), Division of Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo SP 04039-032, Brazil; Center for Applied Genomics (H.H., J.L., R.P.), The Children's Hospital of Philadelphia, Research Institute; and Department of Pediatrics (H.H.), The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.

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http://dx.doi.org/10.1210/jc.2013-2993DOI Listing
June 2014

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.

Nat Commun 2014 Jun 13;5:4074. Epub 2014 Jun 13.

1] The Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA [2] Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1038/ncomms5074DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059929PMC
June 2014

Sleep is not just for the brain: transcriptional responses to sleep in peripheral tissues.

BMC Genomics 2013 May 30;14:362. Epub 2013 May 30.

Division of Sleep Medicine and Center for Sleep and Circadian Neurobiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

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http://dx.doi.org/10.1186/1471-2164-14-362DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701596PMC
May 2013

Autistic disorder phenotype associated to a complex 15q intrachromosomal rearrangement.

Am J Med Genet B Neuropsychiatr Genet 2012 Oct 22;159B(7):823-8. Epub 2012 Aug 22.

Genetics Division, Department of Gynecology and Obstetrics, Faculdade de Medicina do ABC (1) (FMABC), São Paulo, Brazil.

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http://dx.doi.org/10.1002/ajmg.b.32089DOI Listing
October 2012

Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report.

J Med Case Rep 2012 Sep 7;6:283. Epub 2012 Sep 7.

Department of Morphology and Genetics, Universidade Federal de São Paulo, Rua Botucatu 740, São Paulo 04023-900, Brazil.

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http://jmedicalcasereports.biomedcentral.com/articles/10.118
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http://dx.doi.org/10.1186/1752-1947-6-283DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459701PMC
September 2012

Mechanisms of ring chromosome formation, ring instability and clinical consequences.

BMC Med Genet 2011 Dec 21;12:171. Epub 2011 Dec 21.

Genetics Division, Department of Morphology and Genetics, Federal University of São Paulo, Botucatu Street 740, Zip Code 04023-900, São Paulo, Brazil.

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http://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2
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http://dx.doi.org/10.1186/1471-2350-12-171DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309960PMC
December 2011

Trisomy 16q21 --> qter: Seven-year follow-up of a girl with unusually long survival.

Am J Med Genet A 2010 Aug;152A(8):2074-8

Laboratory of Human Genetics and Mutagenesis, Department of General Biology, Universidade Federal da Bahia, Salvador, Bahia, Brazil.

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http://dx.doi.org/10.1002/ajmg.a.33524DOI Listing
August 2010