| Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development M Uda, C Ottolenghi, L Crisponi, JE Garcia, M Deiana, W Kimber, ... Human molecular genetics 13 (11), 1171-1181, 2004 | 797* | 2004 |
| Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. PG Uda M, Ottolenghi C, Crisponi L, Garcia JE, Deiana Hum Mol Genet 13 (11), 1171-1181, 2004 | 617 | 2004 |
| Foxl2 is required for commitment to ovary differentiation C Ottolenghi, S Omari, JE Garcia-Ortiz, M Uda, L Crisponi, A Forabosco, ... Human molecular genetics 14 (14), 2053-2062, 2005 | 379 | 2005 |
| SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome ND Shaw, H Brand, ZA Kupchinsky, H Bengani, L Plummer, TI Jones, ... Nature genetics 49 (2), 238-248, 2017 | 166 | 2017 |
| Alopecia areata: Actualidad y perspectivas KJ Juárez-Rendón, G Rivera Sánchez, MÁ Reyes-López, JE García-Ortiz, ... Archivos argentinos de pediatria 115 (6), e404-e411, 2017 | 122 | 2017 |
| Aging of oocyte, ovary and human reproduction FA Ottolengui C, Uda M, Hamatani T, Crisponi L, Garcia JE, Ko M, Pilia G ... Ann NY Acad Sci 1034, 117-131, 2004 | 108* | 2004 |
| Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia–anophthalmia–coloboma (MAC) spectrum cases J Gonzalez-Rodriguez, EL Pelcastre, JL Tovilla-Canales, JE Garcia-Ortiz, ... British journal of ophthalmology 94 (8), 1100-1104, 2010 | 90 | 2010 |
| Dynamics of the ovarian reserve and impact of genetic and epidemiological factors on age of menopause E Pelosi, E Simonsick, A Forabosco, JE Garcia-Ortiz, D Schlessinger Biology of reproduction 92 (5), 130, 1-9, 2015 | 89 | 2015 |
| A missense mutation, p. V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome LE Becerra‐Solano, J Butler, G Castaneda‐Cisneros, DE McCloskey, ... American Journal of Medical Genetics Part A 149 (3), 328-335, 2009 | 72 | 2009 |
| Paternal determinants in preeclampsia C Galaviz-Hernandez, M Sosa-Macias, E Teran, JE Garcia-Ortiz, ... Frontiers in physiology 9, 1870, 2019 | 71 | 2019 |
| Mouse ovary developmental RNA and protein markers from gene expression profiling L Herrera, C Ottolenghi, JE Garcia-Ortiz, M Pellegrini, F Manini, MSH Ko, ... Developmental Biology 279 (2), 271-290, 2005 | 71 | 2005 |
| Determination and stability of gonadal sex D Schlessinger, JE Garcia‐Ortiz, A Forabosco, M Uda, L Crisponi, ... Journal of andrology 31 (1), 16-25, 2010 | 59 | 2010 |
| High‐resolution molecular characterization of the HLA class I and class II in the Tarahumara Amerindian population JE García‐Ortiz, L Sandoval‐Ramírez, H Rangel‐Villalobos, ... Tissue antigens 68 (2), 135-146, 2006 | 57 | 2006 |
| The association between the 844ins68 polymorphism in the CBS gene and breast cancer M Gallegos-Arreola, LE Figuera-Villanueva, A Ramos-Silva, ... Archives of Medical Science 10 (6), 1214-1224, 2014 | 38 | 2014 |
| Association of the 677C→ T polymorphism in the MTHFR gene with colorectal cancer in Mexican patients MP Gallegos-Arreola, JE Garcia-Ortiz, LE Figuera, AM Puebla-Pérez, ... Cancer Genomics & Proteomics 6 (3), 183-188, 2009 | 37 | 2009 |
| Contribution of CYP1B1 mutations and founder effect to primary congenital glaucoma in Mexico JC Zenteno, E Hernandez-Merino, H Mejia-Lopez, M Matías-Florentino, ... Journal of glaucoma 17 (3), 189-192, 2008 | 31 | 2008 |
| Ring-20-syndrome and loss of telomeric regions D Garcıa-Cruz, AI Vásquez, D Perez-Rulfo, NO Dávalos, JM Penaloza, ... Annales de genetique 43 (3-4), 113-116, 2000 | 30 | 2000 |
| p63 gene analysis in Mexican patients with syndromic and non‐syndromic ectrodactyly V Berdon‐Zapata, M Granillo‐Alvarez, M Valdes‐Flores, JE García‐Ortiz, ... Journal of orthopaedic research 22 (1), 1-5, 2004 | 29 | 2004 |
| Second female case of Myhre syndrome MG Lopez-Cardona, D Garcia-Cruz, JE Garcia-Ortiz, NO Davalos, ... Clinical Dysmorphology 13 (2), 91-94, 2004 | 24 | 2004 |
| Molecular thrombophilic profile in Mexican patients with idiopathic recurrent pregnancy loss JJ López-Jiménez, Á Porras-Dorantes, CI Juárez-Vázquez, ... Genet Mol Res 15 (4), 15048728, 2016 | 23 | 2016 |
