Maria Helena Pinto Azevedo


AuthID: R-001-YR6

Publications Awaiting Confirmation

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TITLE: Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry
AUTHORS: Tim B Bigdeli; Giulio Genovese; Penelope Georgakopoulos; Jacquelyn L Meyers; Roseann E Peterson; Conrad O Iyegbe; Helena Medeiros; Jorge Valderrama; Eric D Achtyes; Roman Kotov; Eli A Stahl; Colony Abbott; Maria Helena Azevedo; Richard A Belliveau; Elizabeth Bevilacqua; Evelyn J Bromet; William Byerley; Celia Barreto Carvalho; Sinead B Chapman; Lynn E DeLisi; Ashley L Dumont; Colm O'Dushlaine; Oleg V Evgrafov; Laura J Fochtmann; Diane Gage; James L Kennedy; Becky Kinkead; Antonio Macedo; Jennifer L Moran; Christopher P Morley; Mantosh J Dewan; James Nemesh; Diana O Perkins; Shaun M Purcell; Jeffrey J Rakofsky; Edward M Scolnick; Brooke M Sklar; Pamela Sklar; Jordan W Smoller; Patrick F Sullivan; Fabio Macciardi; Stephen R Marder; Ruben C Gur; Raquel E Gur; David L Braff; Monica E Calkins; Robert R Freedman; Michael F Green; Tiffany A Greenwood; Laura C Lazzeroni; Gregory A Light; Keith H Nuechterlein; Allen D Radant; Larry J Seidman; Larry J Siever; Jeremy M Silverman; William S Stone; Catherine A Sugar; Neal R Swerdlow; Debby W Tsuang; Ming T Tsuang; Bruce I Turetsky; Humberto Nicolini; Michael A Escamilla; Marquis P Vawter; Janet L Sobell; Dolores Malaspina; Douglas S Lehrer; Peter F Buckley; Mark H Rapaport; James A Knowles; Ayman H Fanous; Michele T Pato; Steven A McCarroll; Carlos N Pato; ...More
PUBLISHED: 2020, SOURCE: MOLECULAR PSYCHIATRY, VOLUME: 25, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 42
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TITLE: MLPA analysis in a cohort of patients with autism  Full Text
AUTHORS: Sara Peixoto; Joana B Melo; Jose Ferrao; Luis M Pires; Nuno Lavoura; Marta Pinto; Guiomar Oliveira; Isabel M Carreira;
PUBLISHED: 2017, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 10, ISSUE: 1
INDEXED IN: Scopus WOS
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TITLE: Prenatal Diagnosis of two rare inv(22) different at molecular level  Full Text
AUTHORS: Melo, JB; Pinto, MC; Jardim, A; Lavoura, N; Pires, LM; Paiva, P; Ramos, F; Simoes, L; Carreira, IM;
PUBLISHED: 2017, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 10
INDEXED IN: WOS
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TITLE: Androgenetic biparental chimerism in prenatal diagnosis a case report  Full Text
AUTHORS: Pinto, MC; Pires, LM; Mascarenhas, A; Jardim, A; Val, M; Paiva, P; Melo, JB; Carreira, IM;
PUBLISHED: 2017, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 10
INDEXED IN: WOS
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TITLE: Molecular characterization of prenatally detected small supernumerary marker chromosomes: improving the genotype-phenotype correlations  Full Text
AUTHORS: Isabel Marques Carreira; Marta Coelho Pinto; Ana Jardim; Susana Isabel Ferreira; Lucia Simoes; Nuno Lavoura; Alexandra Mascarenhas; Eulalia Galhano; Helena Goncalves; Fabiana Ramos; Joana Barbosa Melo;
PUBLISHED: 2015, SOURCE: CHROMOSOME RESEARCH, VOLUME: 23
INDEXED IN: WOS
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TITLE: Association Study of 83 Candidate Genes for Bipolar Disorder in Chromosome 6q Selected Using an Evidence-Based Prioritization Algorithm  Full Text
AUTHORS: Bernard B Bigdeli; Brion S Maher; Zhongming M Zhao; Jingchun C Sun; Helena Medeiros; Nirmala Akula; Francis J McMahon; Celia Carvalho; Susana R Ferreira; Maria H Azevedo; James A Knowles; Michele T Pato; Carlos N Pato; Ayman H Fanous;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, VOLUME: 162, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef
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TITLE: Is haploinsufficiency of SRPK2 gene associated with developmental delay? Report of a de novo 7q22.1q22.3 interstitial deletion  Full Text
AUTHORS: Marta Pinto; Susana Isabel Ferreira; Nuno Lavoura; Alexandra Mascarenhas; Ana Jardim; Ana Beleza Meireles; Isabel Marques Carreira; Joana Barbosa Melo;
PUBLISHED: 2013, SOURCE: CHROMOSOME RESEARCH, VOLUME: 21
INDEXED IN: WOS
Page 1 of 6. Total results: 54.

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