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Angela M. Vianna-Morgante

Angela M. Vianna-Morgante,University of São Paulo,Genetics & Genealogy,Molecular Biology,Cell Biology

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Angela M. Vianna-Morgante

University of São Paulo

Publications: 90 | Citations: 786

Fields: Genetics & Genealogy, Molecular Biology, Cell Biology

Collaborated with 543 co-authors from 1974 to 2010 | Cited by 3447 authors

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Publications (90)

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Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome (Citations: 2)

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Journal: Clinical Genetics - CLIN GENET , vol. 77, no. 4, pp. 404-407, 2010

Posters * Reproductive Genetics (PGD/PGS)

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Journal: Human Reproduction - HUM REPROD , vol. 25, no. Supplement, pp. i321-i332, 2010

Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation

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Journal: American Journal of Medical Genetics Part A - AM J MED GENET PART A , vol. 152A, no. 3, pp. 638-645, 2010

A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation

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Journal: American Journal of Medical Genetics Part A - AM J MED GENET PART A , 2010

An Illustrative Case of Neurofibromatosis Type 1 and NF1 Microdeletion

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Journal: Molecular Syndromology , vol. 1, pp. 133-135, 2010

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Citations (786 times by 690 publications)

Ovarian Abnormalities in a Mouse Model of Fragile X Primary Ovarian Insufficiency

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Journal: Journal of Histochemistry & Cytochemistry - J HISTOCHEM CYTOCHEM , vol. 60, no. 6, pp. 439-456, 2012

Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome

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Journal: PLOS Genetics - PLOS GENET , vol. 8, no. 5, 2012

Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome

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Journal: Nature Genetics - NAT GENET , vol. 44, no. 2, pp. 206-211, 2012

Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms

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Journal: European Journal of Human Genetics - EUR J HUMAN GENET , vol. 20, no. 2, pp. 131-133, 2012

Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature

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Journal: European Journal of Human Genetics - EUR J HUMAN GENET , vol. 20, no. 1, pp. 125-127, 2012

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Co-authors (543)

Journals (25)

Keywords (114)

Angela M. Vianna-Morgante,University of São Paulo,Genetics & Genealogy,Molecular Biology,Cell Biology

Publications (90)

BibTeX | RIS | RefWorks Download

Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome (Citations: 2)

Posters * Reproductive Genetics (PGD/PGS)

Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation

A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation

An Illustrative Case of Neurofibromatosis Type 1 and NF1 Microdeletion

Citations (786 times by 690 publications)

Ovarian Abnormalities in a Mouse Model of Fragile X Primary Ovarian Insufficiency

Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome

Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome

Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms

Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature


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Angela M. Vianna-Morgante,University of São Paulo,Genetics & Genealogy,Molecular Biology,Cell Biology

Publications (90) BibTeX | RIS | RefWorks Download

Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome (Citations: 2)

Publications (90)

BibTeX | RIS | RefWorks Download