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Items: 1 to 50 of 110

1.

Genetic analysis of patients with fructose-1,6-bisphosphatase deficiency.

Pinheiro FC, Sperb-Ludwig F, Ligabue-Braun R, Schüler-Faccini L, de Souza CFM, Vairo F, Schwartz IVD.

Gene. 2019 Mar 9;699:102-109. doi: 10.1016/j.gene.2019.03.007. [Epub ahead of print]

PMID:
30858132
2.

Genetic variants linked to folliculogenesis and successful pregnancy are not associated with twin births in a twins' town.

Cardoso-Dos-Santos AC, Tagliani-Ribeiro A, Matte U, Schuler-Faccini L.

J Matern Fetal Neonatal Med. 2019 Mar 7:1-8. doi: 10.1080/14767058.2019.1573791. [Epub ahead of print]

PMID:
30843750
3.

A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.

Adhikari K, Mendoza-Revilla J, Sohail A, Fuentes-Guajardo M, Lampert J, Chacón-Duque JC, Hurtado M, Villegas V, Granja V, Acuña-Alonzo V, Jaramillo C, Arias W, Lozano RB, Everardo P, Gómez-Valdés J, Villamil-Ramírez H, Silva de Cerqueira CC, Hunemeier T, Ramallo V, Schuler-Faccini L, Salzano FM, Gonzalez-José R, Bortolini MC, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Tobin DJ, Fumagalli M, Balding D, Ruiz-Linares A.

Nat Commun. 2019 Jan 21;10(1):358. doi: 10.1038/s41467-018-08147-0.

4.

ADGRL3 rs6551665 as a Common Vulnerability Factor Underlying Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder.

Kappel DB, Schuch JB, Rovaris DL, da Silva BS, Müller D, Breda V, Teche SP, S Riesgo R, Schüler-Faccini L, Rohde LA, Grevet EH, Bau CHD.

Neuromolecular Med. 2019 Mar;21(1):60-67. doi: 10.1007/s12017-019-08525-x. Epub 2019 Jan 16.

PMID:
30652248
5.

Zika Virus as a Possible Risk Factor for Autism Spectrum Disorder: Neuroimmunological Aspects.

Vianna P, Gomes JDA, Boquett JA, Fraga LR, Schuch JB, Vianna FSL, Schuler-Faccini L.

Neuroimmunomodulation. 2018;25(5-6):320-327. doi: 10.1159/000495660. Epub 2019 Jan 10. Review.

6.

Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance.

Chacón-Duque JC, Adhikari K, Fuentes-Guajardo M, Mendoza-Revilla J, Acuña-Alonzo V, Barquera R, Quinto-Sánchez M, Gómez-Valdés J, Everardo Martínez P, Villamil-Ramírez H, Hünemeier T, Ramallo V, Silva de Cerqueira CC, Hurtado M, Villegas V, Granja V, Villena M, Vásquez R, Llop E, Sandoval JR, Salazar-Granara AA, Parolin ML, Sandoval K, Peñaloza-Espinosa RI, Rangel-Villalobos H, Winkler CA, Klitz W, Bravi C, Molina J, Corach D, Barrantes R, Gomes V, Resende C, Gusmão L, Amorim A, Xue Y, Dugoujon JM, Moral P, González-José R, Schuler-Faccini L, Salzano FM, Bortolini MC, Canizales-Quinteros S, Poletti G, Gallo C, Bedoya G, Rothhammer F, Balding D, Hellenthal G, Ruiz-Linares A.

Nat Commun. 2018 Dec 19;9(1):5388. doi: 10.1038/s41467-018-07748-z.

7.

Lack of association between genetic polymorphisms in IGF1 and IGFBP3 with twin births in a Brazilian population (Cândido Godói, Rio Grande do Sul).

Oliveira-Klein M, Cardoso-Dos-Santos AC, Tagliani-Ribeiro A, Fagundes NR, Matte U, Schuler-Faccini L.

Genet Mol Biol. 2018 Oct-Dec;41(4):775-780. doi: 10.1590/1678-4685-GMB-2017-0263. Epub 2018 Nov 29.

8.

Is intrauterine exposure to acetaminophen associated with emotional and hyperactivity problems during childhood? Findings from the 2004 Pelotas birth cohort.

Tovo-Rodrigues L, Schneider BC, Martins-Silva T, Del-Ponte B, Loret de Mola C, Schuler-Faccini L, Vianna FSL, Munhoz TN, Entiauspe L, Silveira MF, Santos IS, Matijasevich A, Barros AJD, Rohde LA, Bertoldi AD.

BMC Psychiatry. 2018 Nov 20;18(1):368. doi: 10.1186/s12888-018-1942-1.

9.

Profile of congenital anomalies among live births in the municipality of Tangará da Serra, Mato Grosso, Brazil, 2006-2016.

Silva JHD, Terças ACP, Pinheiro LCB, França GVA, Atanaka M, Schüler-Faccini L.

Epidemiol Serv Saude. 2018 Oct 22;27(3):e2018008. doi: 10.5123/S1679-49742018000300017. English, Portuguese.

10.

Collagen I Defect Corneal Profiles in Osteogenesis Imperfecta.

Magalhaes OA, Rohenkohl HC, de Souza LT, Schuler-Faccini L, Félix TM.

Cornea. 2018 Dec;37(12):1561-1565. doi: 10.1097/ICO.0000000000001764.

PMID:
30272615
11.

Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans.

Wu S, Zhang M, Yang X, Peng F, Zhang J, Tan J, Yang Y, Wang L, Hu Y, Peng Q, Li J, Liu Y, Guan Y, Chen C, Hamer MA, Nijsten T, Zeng C, Adhikari K, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, González-José R, Li H, Krutmann J, Liu F, Kayser M, Ruiz-Linares A, Tang K, Xu S, Zhang L, Jin L, Wang S.

PLoS Genet. 2018 Sep 24;14(9):e1007640. doi: 10.1371/journal.pgen.1007640. eCollection 2018 Sep.

12.

Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.

Moorthie S, Blencowe H, Darlison MW, Lawn J, Morris JK, Modell B; Congenital Disorders Expert Group , Bittles AH, Blencowe H, Christianson A, Cousens S, Darlison MW, Gibbons S, Hamamy H, Khoshnood B, Howson CP, Lawn J, Mastroiacovo P, Modell B, Moorthie S, Morris JK, Mossey PA, Neville AJ, Petrou M, Povey S, Rankin J, Schuler-Faccini L, Wren C, Yunnis KA.

J Community Genet. 2018 Oct;9(4):387-396. doi: 10.1007/s12687-018-0384-2. Epub 2018 Sep 14.

13.

Spatial analyzes of HLA data in Rio Grande do Sul, south Brazil: genetic structure and possible correlation with autoimmune diseases.

Boquett JA, Zagonel-Oliveira M, Jobim LF, Jobim M, Gonzaga L Jr, Veronez MR, Fagundes NJR, Schüler-Faccini L.

Int J Health Geogr. 2018 Sep 14;17(1):34. doi: 10.1186/s12942-018-0154-8.

14.

Intrafamilial clinical variability in four families with incontinentia pigmenti.

Mariath LM, Santa Maria FD, Poziomczyk CS, Travi GM, Wachholz GE, De Souza SR, Kiszewski AE, Schuler-Faccini L.

Am J Med Genet A. 2018 Nov;176(11):2318-2324. doi: 10.1002/ajmg.a.40497. Epub 2018 Aug 27.

PMID:
30151858
15.

Why is congenital Zika syndrome asymmetrically distributed among human populations?

Barbeito-Andrés J, Schuler-Faccini L, Garcez PP.

PLoS Biol. 2018 Aug 24;16(8):e2006592. doi: 10.1371/journal.pbio.2006592. eCollection 2018 Aug.

16.

Twin Peaks: A spatial and temporal study of twinning rates in Brazil.

Cardoso-Dos-Santos AC, Boquett J, Oliveira MZ, Callegari-Jacques SM, Barbian MH, Sanseverino MTV, Matte U, Schuler-Faccini L.

PLoS One. 2018 Jul 20;13(7):e0200885. doi: 10.1371/journal.pone.0200885. eCollection 2018.

17.

Clusters of genetic diseases in Brazil.

Cardoso GC, de Oliveira MZ, Paixão-Côrtes VR, Castilla EE, Schuler-Faccini L.

J Community Genet. 2019 Jan;10(1):121-128. doi: 10.1007/s12687-018-0369-1. Epub 2018 Jun 2.

18.

Evidence for Association Between OXTR Gene and ASD Clinical Phenotypes.

de Oliveira Pereira Ribeiro L, Vargas-Pinilla P, Kappel DB, Longo D, Ranzan J, Becker MM, Dos Santos Riesgo R, Schuler-Faccini L, Roman T, Schuch JB.

J Mol Neurosci. 2018 Jun;65(2):213-221. doi: 10.1007/s12031-018-1088-0. Epub 2018 Jun 1.

PMID:
29858823
19.

Erythema Nodosum Leprosum: Update and challenges on the treatment of a neglected condition.

Costa PDSS, Fraga LR, Kowalski TW, Daxbacher ELR, Schuler-Faccini L, Vianna FSL.

Acta Trop. 2018 Jul;183:134-141. doi: 10.1016/j.actatropica.2018.02.026. Epub 2018 Feb 21. Review.

PMID:
29474830
20.

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.

Shaffer JR, Li J, Lee MK, Roosenboom J, Orlova E, Adhikari K; 23andMe Research Team, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, González-José R, Pfeffer PE, Wollenschlaeger CA, Hecht JT, Wehby GL, Moreno LM, Ding A, Jin L, Yang Y, Carlson JC, Leslie EJ, Feingold E, Marazita ML, Hinds DA, Cox TC, Wang S, Ruiz-Linares A, Weinberg SM.

Am J Hum Genet. 2017 Dec 7;101(6):913-924. doi: 10.1016/j.ajhg.2017.10.001. Epub 2017 Nov 30.

21.

Genetic susceptibility to thalidomide embryopathy in humans: Study of candidate development genes.

Gomes JDA, Kowalski TW, Fraga LR, Tovo-Rodrigues L, Sanseverino MTV, Schuler-Faccini L, Vianna FSL.

Birth Defects Res. 2018 Mar 15;110(5):456-461. doi: 10.1002/bdr2.1163. Epub 2017 Nov 28.

PMID:
29193903
22.

Angiogenesis and oxidative stress-related gene variants in recurrent pregnancy loss.

Fortis MF, Fraga LR, Boquett JA, Kowalski TW, Dutra CG, Gonçalves RO, Vianna FSL, Schüler-Faccini L, Sanseverino MTV.

Reprod Fertil Dev. 2018 Mar;30(3):498-506. doi: 10.1071/RD17117.

PMID:
28825972
23.

Leprosy in Southern Brazil: a twenty-year epidemiological profile.

Nazario AP, Ferreira J, Schuler-Faccini L, Fiegenbaum M, Artigalás O, Vianna FSL.

Rev Soc Bras Med Trop. 2017 Mar-Apr;50(2):251-255. doi: 10.1590/0037-8682-0229-2016.

24.

Teratogens: a public health issue - a Brazilian overview.

Mazzu-Nascimento T, Melo DG, Morbioli GG, Carrilho E, Vianna FSL, Silva AA, Schuler-Faccini L.

Genet Mol Biol. 2017 Apr-Jun;40(2):387-397. doi: 10.1590/1678-4685-GMB-2016-0179. Epub 2017 May 22.

25.

Music genetics research: Association with musicality of a polymorphism in the AVPR1A gene.

Mariath LM, Silva AM, Kowalski TW, Gattino GS, Araujo GA, Figueiredo FG, Tagliani-Ribeiro A, Roman T, Vianna FSL, Schuler-Faccini L, Schuch JB.

Genet Mol Biol. 2017 Apr-Jun;40(2):421-429. doi: 10.1590/1678-4685-GMB-2016-0021. Epub 2017 May 22.

26.

The phenotypic spectrum of congenital Zika syndrome.

Del Campo M, Feitosa IM, Ribeiro EM, Horovitz DD, Pessoa AL, França GV, García-Alix A, Doriqui MJ, Wanderley HY, Sanseverino MV, Neri JI, Pina-Neto JM, Santos ES, Verçosa I, Cernach MC, Medeiros PF, Kerbage SC, Silva AA, van der Linden V, Martelli CM, Cordeiro MT, Dhalia R, Vianna FS, Victora CG, Cavalcanti DP, Schuler-Faccini L; Zika Embryopathy Task Force-Brazilian Society of Medical Genetics ZETF-SBGM.

Am J Med Genet A. 2017 Apr;173(4):841-857. doi: 10.1002/ajmg.a.38170.

PMID:
28328129
27.

Correction: Socioeconomic Status Is Not Related with Facial Fluctuating Asymmetry: Evidence from Latin-American Populations.

Quinto-Sánchez M, Cintas C, Silva de Cerqueira CC, Ramallo V, Acuña-Alonzo V, Adhikari K, Castillo L, Gomez-Valdés J, Everardo P, De Avila F, Hünemeier T, Jaramillo C, Arias W, Fuentes M, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, Rosique J, Ruiz-Linares A, González-José R.

PLoS One. 2017 Feb 13;12(2):e0172418. doi: 10.1371/journal.pone.0172418. eCollection 2017.

28.

ZIKA Virus and Neuroscience: the Need for a Translational Collaboration.

Schuler-Faccini L, Roehe P, Zimmer ER, Quincozes-Santos A, de Assis AM, Lima EOC, Guimarães JA, Victora C, Neto VM, Souza DO.

Mol Neurobiol. 2018 Feb;55(2):1551-1555. doi: 10.1007/s12035-017-0429-2. Epub 2017 Feb 9.

PMID:
28185126
29.

Analysis of Polymorphism rs1042522 in TP53 Gene in the Mothers of Twins and of Singletons: A Population-Based Study in Rio Grande do Sul, Brazil.

Mardini AC, Pereira FS, Schuler-Faccini L, Matte U.

Twin Res Hum Genet. 2017 Apr;20(2):132-136. doi: 10.1017/thg.2017.2. Epub 2017 Feb 9.

PMID:
28179045
30.

Angiogenesis-related genes and thalidomide teratogenesis in humans: an approach on genetic variation and review of past in vitro studies.

Kowalski TW, Fraga LR, Tovo-Rodrigues L, Sanseverino MTV, Hutz MH, Schuler-Faccini L, Vianna FSL.

Reprod Toxicol. 2017 Jun;70:133-140. doi: 10.1016/j.reprotox.2017.01.012. Epub 2017 Feb 1.

PMID:
28161597
31.

Zika rash and increased risk of congenital brain abnormalities - Authors' reply.

Victora CG, Castro MC, França GV, Schuler-Faccini L, Barros FC.

Lancet. 2017 Jan 14;389(10065):152. doi: 10.1016/S0140-6736(17)30015-6. Epub 2017 Jan 13. No abstract available.

PMID:
28102136
32.

Socioeconomic Status Is Not Related with Facial Fluctuating Asymmetry: Evidence from Latin-American Populations.

Quinto-Sánchez M, Cintas C, Silva de Cerqueira CC, Ramallo V, Acuña-Alonzo V, Adhikari K, Castillo L, Gomez-Valdés J, Everardo P, De Avila F, Hünemeier T, Jaramillo C, Arias W, Fuentes M, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, Rosique J, Ruiz-Linares A, González-José R.

PLoS One. 2017 Jan 6;12(1):e0169287. doi: 10.1371/journal.pone.0169287. eCollection 2017. Erratum in: PLoS One. 2017 Feb 13;12 (2):e0172418.

33.

The HLA-A, -B and -DRB1 polymorphism in a large dataset of South Brazil bone marrow donors from Rio Grande do Sul.

Boquett JA, Nunes JM, Buhler S, de Oliveira MZ, Jobim LF, Jobim M, Fagundes NJ, Schüler-Faccini L, Sanchez-Mazas A.

HLA. 2017 Jan;89(1):29-38. doi: 10.1111/tan.12933. Epub 2016 Dec 2.

PMID:
27910249
34.

Genomic and in silico analyses of CRBN gene and thalidomide embryopathy in humans.

Vianna FS, Kowalski TW, Tovo-Rodrigues L, Tagliani-Ribeiro A, Godoy BA, Fraga LR, Sanseverino MT, Hutz MH, Schuler-Faccini L.

Reprod Toxicol. 2016 Dec;66:99-106. doi: 10.1016/j.reprotox.2016.10.003. Epub 2016 Oct 14.

PMID:
27751757
35.

The impact of thalidomide use in birth defects in Brazil.

Sales Luiz Vianna F, Kowalski TW, Fraga LR, Sanseverino MT, Schuler-Faccini L.

Eur J Med Genet. 2017 Jan;60(1):12-15. doi: 10.1016/j.ejmg.2016.09.015. Epub 2016 Sep 13.

PMID:
27638330
36.

Association between the thrombophilic polymorphisms MTHFR C677T, Factor V Leiden, and prothrombin G20210A and recurrent miscarriage in Brazilian women.

Gonçalves RO, Fraga LR, Santos WV, Carvalho AF, Veloso Cerqueira BA, Sarno M, Toralles MB, Vieira MJ, Dutra CG, Schüler-Faccini L, Sanseverino MT, Gonçalves MS, Vianna FS, Costa OL.

Genet Mol Res. 2016 Jul 15;15(3). doi: 10.4238/gmr.15038156.

PMID:
27525841
37.

Congenital Zika virus syndrome in Brazil: a case series of the first 1501 livebirths with complete investigation.

França GV, Schuler-Faccini L, Oliveira WK, Henriques CM, Carmo EH, Pedi VD, Nunes ML, Castro MC, Serruya S, Silveira MF, Barros FC, Victora CG.

Lancet. 2016 Aug 27;388(10047):891-7. doi: 10.1016/S0140-6736(16)30902-3. Epub 2016 Jun 29.

38.

Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil.

Palmero EI, Alemar B, Schüler-Faccini L, Hainaut P, Moreira-Filho CA, Ewald IP, Santos PK, Ribeiro PL, Oliveira CB, Calvez-Kelm FL, Tavtigian S, Cossio SL, Giugliani R, Caleffi M, Ashton-Prolla P.

Genet Mol Biol. 2016 May 24;39(2):210-22. doi: 10.1590/1678-4685-GMB-2014-0363. Erratum in: Genet Mol Biol. 2017 Mar 16;:0.

39.

A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.

Adhikari K, Fuentes-Guajardo M, Quinto-Sánchez M, Mendoza-Revilla J, Camilo Chacón-Duque J, Acuña-Alonzo V, Jaramillo C, Arias W, Lozano RB, Pérez GM, Gómez-Valdés J, Villamil-Ramírez H, Hunemeier T, Ramallo V, Silva de Cerqueira CC, Hurtado M, Villegas V, Granja V, Gallo C, Poletti G, Schuler-Faccini L, Salzano FM, Bortolini MC, Canizales-Quinteros S, Cheeseman M, Rosique J, Bedoya G, Rothhammer F, Headon D, González-José R, Balding D, Ruiz-Linares A.

Nat Commun. 2016 May 19;7:11616. doi: 10.1038/ncomms11616.

40.

Zika virus: A new human teratogen? Implications for women of reproductive age.

Schuler-Faccini L, Sanseverino M, Vianna F, da Silva AA, Larrandaburu M, Marcolongo-Pereira C, Abeche AM.

Clin Pharmacol Ther. 2016 Jul;100(1):28-30. doi: 10.1002/cpt.386. Epub 2016 May 13.

PMID:
27090438
41.

Retinoblastoma in a pediatric oncology reference center in Southern Brazil.

Selistre SGA, Maestri MK, Santos-Silva P, Schüler-Faccini L, Guimarães LSP, Giacomazzi J, Evangelista Júnior MC, Ashton-Prolla P.

BMC Pediatr. 2016 Apr 3;16:48. doi: 10.1186/s12887-016-0579-9.

42.

New Findings in eNOS gene and Thalidomide Embryopathy Suggest pre-transcriptional effect variants as susceptibility factors.

Kowalski TW, Fraga LR, Tovo-Rodrigues L, Sanseverino MT, Hutz MH, Schuler-Faccini L, Vianna FS.

Sci Rep. 2016 Mar 23;6:23404. doi: 10.1038/srep23404.

43.

A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.

Adhikari K, Fontanil T, Cal S, Mendoza-Revilla J, Fuentes-Guajardo M, Chacón-Duque JC, Al-Saadi F, Johansson JA, Quinto-Sanchez M, Acuña-Alonzo V, Jaramillo C, Arias W, Barquera Lozano R, Macín Pérez G, Gómez-Valdés J, Villamil-Ramírez H, Hunemeier T, Ramallo V, Silva de Cerqueira CC, Hurtado M, Villegas V, Granja V, Gallo C, Poletti G, Schuler-Faccini L, Salzano FM, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, Gonzalez-José R, Headon D, López-Otín C, Tobin DJ, Balding D, Ruiz-Linares A.

Nat Commun. 2016 Mar 1;7:10815. doi: 10.1038/ncomms10815.

44.

Microcephaly in Brazil: how to interpret reported numbers?

Victora CG, Schuler-Faccini L, Matijasevich A, Ribeiro E, Pessoa A, Barros FC.

Lancet. 2016 Feb 13;387(10019):621-4. doi: 10.1016/S0140-6736(16)00273-7. Epub 2016 Feb 7. No abstract available.

PMID:
26864961
45.

Possible Association Between Zika Virus Infection and Microcephaly - Brazil, 2015.

Schuler-Faccini L, Ribeiro EM, Feitosa IM, Horovitz DD, Cavalcanti DP, Pessoa A, Doriqui MJ, Neri JI, Neto JM, Wanderley HY, Cernach M, El-Husny AS, Pone MV, Serao CL, Sanseverino MT; Brazilian Medical Genetics Society–Zika Embryopathy Task Force.

MMWR Morb Mortal Wkly Rep. 2016 Jan 29;65(3):59-62. doi: 10.15585/mmwr.mm6503e2.

46.

Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions.

Souza GN, Kersting N, Krum-Santos AC, Santos AS, Furtado GV, Pacheco D, Gonçalves TA, Saute JA, Schuler-Faccini L, Mattos EP, Saraiva-Pereira ML, Jardim LB.

Clin Genet. 2016 Aug;90(2):134-40. doi: 10.1111/cge.12719. Epub 2016 Feb 3.

PMID:
26693702
47.

Primary prevention of neural tube defects in Brazil: insights into anencephaly.

Bronberg R, Dipierri J, Alfaro E, Sanseverino MT, Schüler-Faccini L.

J Community Genet. 2016 Jan;7(1):97-105. doi: 10.1007/s12687-015-0249-x. Epub 2015 Aug 18. No abstract available.

48.

A genome-wide association study identifies multiple loci for variation in human ear morphology.

Adhikari K, Reales G, Smith AJ, Konka E, Palmen J, Quinto-Sanchez M, Acuña-Alonzo V, Jaramillo C, Arias W, Fuentes M, Pizarro M, Barquera Lozano R, Macín Pérez G, Gómez-Valdés J, Villamil-Ramírez H, Hunemeier T, Ramallo V, Silva de Cerqueira CC, Hurtado M, Villegas V, Granja V, Gallo C, Poletti G, Schuler-Faccini L, Salzano FM, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, Calderón R, Rosique J, Cheeseman M, Bhutta MF, Humphries SE, Gonzalez-José R, Headon D, Balding D, Ruiz-Linares A.

Nat Commun. 2015 Jun 24;6:7500. doi: 10.1038/ncomms8500.

49.

Thalidomide embryopathy: Follow-up of cases born between 1959 and 2010.

Kowalski TW, Sanseverino MT, Schuler-Faccini L, Vianna FS.

Birth Defects Res A Clin Mol Teratol. 2015 Sep;103(9):794-803. doi: 10.1002/bdra.23376. Epub 2015 Jun 4.

PMID:
26043318
50.

Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm.

Larrandaburu M, Matte U, Noble A, Olivera Z, Sanseverino MT, Nacul L, Schuler-Faccini L.

J Community Genet. 2015 Jul;6(3):241-9. doi: 10.1007/s12687-015-0236-2. Epub 2015 May 29.

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