Regina Celia Mingroni Netto
Regina Celia Mingroni Netto
Professor Associado Instituto de Biociências da Universidade de São Paulo
Verified email at ib.usp.br
Title
Cited by
Cited by
Year
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study—preliminary data
DJ Allingham‐Hawkins, R Babul‐Hirji, D Chitayat, JJA Holden, KT Yang, ...
American journal of medical genetics 83 (4), 322-325, 1999
5111999
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations
ACV Krepischi-Santos, AM Vianna-Morgante, FS Jehee, ...
Cytogenetic and genome research 115 (3-4), 254-261, 2006
1272006
A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males
LA Haddad, RC Mingroni-Netto, AM Vianna-Morgante, SDJ Pena
Human genetics 97 (6), 808-812, 1996
871996
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
E Klopocki, S Lohan, SC Doelken, S Stricker, CW Ockeloen, ...
Journal of medical genetics 49 (2), 119-125, 2012
802012
Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling
AC Batissoco, RS Abreu-Silva, MCC Braga, K Lezirovitz, V Della-Rosa, ...
Ear and hearing 30 (1), 1-7, 2009
802009
Report of a del22q11 in a patient with Mayer‐Rokitansky‐Küster‐Hauser (MRKH) anomaly and exclusion of WNT‐4, RAR‐gamma, and RXR‐alpha as major …
C Cheroki, AC Krepischi‐Santos, C Rosenberg, FS Jehee, ...
American Journal of Medical Genetics Part A 140 (12), 1339-1342, 2006
712006
Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness
K Lezirovitz, E Pardono, MTB de Mello Auricchio, FLC e Silva, JJ Lopes, ...
European Journal of Human Genetics 16 (1), 89-96, 2008
602008
Novel OTOF mutations in Brazilian patients with auditory neuropathy
J Romanos, L Kimura, ML Fávero, FAR Izarra, MTB de Mello Auricchio, ...
Journal of human genetics 54 (7), 382-385, 2009
532009
The search of a genetic basis for noise-induced hearing loss (NIHL)
RS Abreu-Silva, D Rincon, ARVR Horimoto, AP Sguillar, LAC Ricardo, ...
Annals of Human Biology 38 (2), 210-218, 2011
512011
Prevalence of the A1555G (12S rRNA) and tRNA Ser (UCN) mitochondrial mutations in hearing-impaired Brazilian patients
RS Abreu-Silva, K Lezirovitz, MCC Braga, M Spinelli, S Pirana, ...
Brazilian journal of medical and biological research 39 (2), 219-226, 2006
502006
Multilocus analyses of seven candidate genes suggest interacting pathways for obesity‐related traits in Brazilian populations
CB Angeli, L Kimura, MT Auricchio, JP Vicente, VS Mattevi, ...
Obesity 19 (6), 1244-1251, 2011
482011
A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians
KS Vimaleswaran, V Radha, K Ramya, HNS Babu, N Savitha, V Roopa, ...
Human Genetics 123 (6), 599, 2008
452008
Frequency and origins of hemoglobin S mutation in African-derived Brazilian populations
MTB de Mello Auricchio, JP Vicente, D Meyer, RC Mingroni-Netto
Human biology 79 (6), 667-677, 2007
402007
Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population
L Kimura, CB Angeli, M Auricchio, GR Fernandes, AC Pereira, JP Vicente, ...
International journal of hypertension 2012, 2012
392012
A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13. 1–17p13. 3
K Lezirovitz, SRP Maestrelli, NH Cotrim, PA Otto, PL Pearson, ...
Human genetics 123 (6), 625, 2008
382008
Genomic ancestry of rural African‐derived populations from Southeastern Brazil
L Kimura, EM Ribeiro‐Rodrigues, MTB De Mello Auricchio, JP Vicente, ...
American Journal of Human Biology 25 (1), 35-41, 2013
342013
Fully mutated and gray‐zone FRAXA alleles in Brazilian mentally retarded boys
LA Haddad, MJB Aguiar, SS Costa, RC Mingroni‐Netto, ...
American journal of medical genetics 84 (3), 198-201, 1999
341999
ADRB2 and LEPR Gene Polymorphisms: Synergistic Effects on the Risk of Obesity in Japanese
TV Pereira, RC Mingroni‐Netto, Y Yamada
Obesity 19 (7), 1523-1527, 2011
292011
Polymorphic Alu insertions in six Brazilian African‐derived populations
NH Cotrim, MTBM Auricchio, JP Vicente, PA Otto, RC Mingroni‐Netto
American Journal of Human Biology: The Official Journal of the Human Biology …, 2004
292004
Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations
RC Mingroni‐Netto, CB Angeli, MTBM Auricchio, ER Leal‐Mesquita, ...
American journal of medical genetics 111 (3), 243-252, 2002
292002
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