متابعة
Regina Celia Mingroni Netto
Regina Celia Mingroni Netto
Professor Associado Instituto de Biociências da Universidade de São Paulo
بريد إلكتروني تم التحقق منه على ib.usp.br
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
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
5811999
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
1412006
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
1052012
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
1012009
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, 808-812, 1996
931996
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
842006
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
MS Naslavsky, MO Scliar, GL Yamamoto, JYT Wang, S Zverinova, T Karp, ...
Nature communications 13 (1), 1004, 2022
712022
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
682009
Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness
K Lezirovitz, E Pardono, MTB de Mello Auricchio, FL de Carvalho e Silva, ...
European Journal of Human Genetics 16 (1), 89-96, 2008
672008
Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities
N Sobreira, M Brucato, L Zhang, C Ladd-Acosta, C Ongaco, J Romm, ...
European Journal of Human Genetics 25 (12), 1335-1344, 2017
602017
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
592011
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
562012
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
532011
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, 219-226, 2006
512006
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, 625-631, 2008
462008
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
462007
Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration
LV Pereira, RF Bento, DB Cruz, C Marchi, R Salomone, J Oiticicca, ...
Cell Transplantation 28 (1), 55-64, 2019
452019
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
442013
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
411999
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
402011
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مقالات 1–20