Works by Zenteno, Juan C.

Results: 40
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    Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 689, doi. 10.1038/ng0615-689c
    By:
    • Aung, Tin;
    • Ozaki, Mineo;
    • Mizoguchi, Takanori;
    • Allingham, R Rand;
    • Li, Zheng;
    • Haripriya, Aravind;
    • Nakano, Satoko;
    • Uebe, Steffen;
    • Harder, Jeffrey M;
    • Chan, Anita S Y;
    • Lee, Mei Chin;
    • Burdon, Kathryn P;
    • Astakhov, Yury S;
    • Abu-Amero, Khaled K;
    • Zenteno, Juan C;
    • Nilgün, Yildirim;
    • Zarnowski, Tomasz;
    • Pakravan, Mohammad;
    • Safieh, Leen Abu;
    • Jia, Liyun
    Publication type:
    Article
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    A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

    Published in:
    Nature Genetics, 2015, v. 47, n. 4, p. 387, doi. 10.1038/ng.3226
    By:
    • Aung, Tin;
    • Chan, Anita S Y;
    • Perera, Shamira A;
    • Husain, Rahat;
    • Lee, Mei Chin;
    • Vithana, Eranga N;
    • Burdon, Kathryn P;
    • Astakhov, Yury S;
    • Astakhov, Sergei Y;
    • Akopov, Evgeny L;
    • Abu-Amero, Khaled K;
    • Zenteno, Juan C;
    • Guadarrama-Vallejo, Dalia;
    • Nilgün, Yildirim;
    • Yetkin, Yaz;
    • Oğuz, Çilingir;
    • Zarnowski, Tomasz;
    • Kosior-Jarecka, Ewa;
    • Lukasik, Urszula;
    • Pakravan, Mohammad
    Publication type:
    Article
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    Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation.

    Published in:
    American Journal of Medical Genetics. Part A, 2020, v. 182, n. 5, p. 1223, doi. 10.1002/ajmg.a.61506
    By:
    • Acosta‐Fernández, Elizabeth;
    • Zenteno, Juan C.;
    • Chacón‐Camacho, Oscar F.;
    • Peña‐Padilla, Christian;
    • Bobadilla‐Morales, Lucina;
    • Corona‐Rivera, Alfredo;
    • Romo‐Huerta, Carmen O.;
    • Zepeda‐Romero, Luz C.;
    • López‐Marure, Eloy;
    • Acosta‐León, Jorge;
    • García‐Cruz, Diana;
    • Maciel‐Cruz, Eric Jonathan;
    • Corona‐Rivera, Jorge Román
    Publication type:
    Article
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    Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratoma.

    Published in:
    American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2710, doi. 10.1002/ajmg.a.40644
    By:
    • Blackburn, Patrick R.;
    • Chacon‐Camacho, Oscar F.;
    • Ortiz‐González, Xilma R.;
    • Reyes, Mariana;
    • Lopez‐Uriarte, Graciela A.;
    • Zarei, Shabnam;
    • Bhoj, Elizabeth J.;
    • Perez‐Solorzano, Sofia;
    • Vaubel, Rachael A.;
    • Murphree, Marine I.;
    • Nava, Jessica;
    • Cortes‐Gonzalez, Vianney;
    • Parisi, Joseph E.;
    • Villanueva‐Mendoza, Cristina;
    • Tirado‐Torres, Iris G.;
    • Li, Dong;
    • Klee, Eric W.;
    • Pichurin, Pavel N.;
    • Zenteno, Juan C.
    Publication type:
    Article
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    Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1002/mgg3.1044
    By:
    • Zenteno, Juan C.;
    • García‐Montaño, Leopoldo A.;
    • Cruz‐Aguilar, Marisa;
    • Ronquillo, Josué;
    • Rodas‐Serrano, Agustín;
    • Aguilar‐Castul, Luis;
    • Matsui, Rodrigo;
    • Vencedor‐Meraz, Carlos I.;
    • Arce‐González, Rocío;
    • Graue‐Wiechers, Federico;
    • Gutiérrez‐Paz, Mario;
    • Urrea‐Victoria, Tatiana;
    • Dios Cuadras, Ulises;
    • Chacón‐Camacho, Oscar F.
    Publication type:
    Article
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    protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 15, p. 2531, doi. 10.1093/hmg/ddz075
    By:
    • Berner, Daniel;
    • Hoja, Ursula;
    • Zenkel, Matthias;
    • Ross, James Julian;
    • Uebe, Steffen;
    • Paoli, Daniela;
    • Frezzotti, Paolo;
    • Rautenbach, Robyn M;
    • Ziskind, Ari;
    • Williams, Susan E;
    • Carmichael, Trevor R;
    • Ramsay, Michele;
    • Topouzis, Fotis;
    • Chatzikyriakidou, Anthi;
    • Lambropoulos, Alexandros;
    • Sundaresan, Periasamy;
    • Ayub, Humaira;
    • Akhtar, Farah;
    • Qamar, Raheel;
    • Zenteno, Juan C
    Publication type:
    Article