| Molecular analyses of 17p11. 2 deletions in 62 Smith-Magenis syndrome patients. RC Juyal, LE Figuera, X Hauge, SH Elsea, JR Lupski, F Greenberg, ... American journal of human genetics 58 (5), 998, 1996 | 165 | 1996 |
| Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum B Struk, L Cai, S Zäch, W Ji, J Chung, A Lumsden, M Stumm, M Huber, ... Journal of molecular medicine 78, 282-286, 2000 | 162 | 2000 |
| Effects of enzyme replacement therapy in Fabry disease—a comprehensive review of the medical literature O Lidove, ML West, G Pintos-Morell, R Reisin, K Nicholls, LE Figuera, ... Genetics in Medicine 12 (11), 668-679, 2010 | 153 | 2010 |
| Association of β-defensin 1 single nucleotide polymorphisms with atopic dermatitis E Prado-Montes de Oca, A García-Vargas, R Lozano-Inocencio, ... International archives of allergy and immunology 142 (3), 211-218, 2007 | 87 | 2007 |
| A 500-kb region on chromosome 16p13. 1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structure L Cai, B Struk, MD Adams, W Ji, T Haaf, HL Kang, SH Dho, X Xu, ... Journal of molecular medicine 78, 36-46, 2000 | 86 | 2000 |
| Mutation of SDHB is a Cause of Hypoxia-Related High-Altitude Paraganglioma NY Cerecer-Gil, LE Figuera, FJ Llamas, M Lara, JG Escamilla, R Ramos, ... Clinical Cancer Research 16 (16), 4148-4154, 2010 | 81 | 2010 |
| Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24–q27. 1 LE Figuera, M Pandolfo, PW Dunne, JM Cantú, PI Patel Nature genetics 10 (2), 202-207, 1995 | 80 | 1995 |
| SNP 668C (− 44) alters a NF-κB1 putative binding site in non-coding strand of human β-defensin 1 (DEFB1) and is associated with lepromatous leprosy EPM de Oca, JS Velarde-Félix, JJ Ríos-Tostado, VJ Picos-Cárdenas, ... Infection, Genetics and Evolution 9 (4), 617-625, 2009 | 74 | 2009 |
| Urinary glycosaminoglycan excretion in healthy subjects and in patients with mucopolysaccharidoses MP Gallegos-Arreola, MV Machorro-Lazo, SE Flores-Martı́nez, ... Archives of medical research 31 (5), 505-510, 2000 | 74 | 2000 |
| X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3 H Zhu, D Shang, M Sun, S Choi, Q Liu, J Hao, LE Figuera, F Zhang, ... The American Journal of Human Genetics 88 (6), 819-826, 2011 | 66 | 2011 |
| 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 | 59 | 2006 |
| Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia IP Davalos, MC Moran, E Martinez-Abundis, M Gonzalez-Ortiz, ... Blood Cells, Molecules, and Diseases 35 (1), 66-69, 2005 | 59 | 2005 |
| Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases JP Mena, M Salazar-Páramo, L González-López, JI Gámez-Nava, ... The Pharmacogenomics Journal 11 (4), 287-291, 2011 | 57 | 2011 |
| Inherited hypertrichoses D Garcia‐Cruz, LE Figuera, JM Cantu Clinical genetics 61 (5), 321-329, 2002 | 56 | 2002 |
| Therapeutic goals in the treatment of Fabry disease A Mehta, ML West, G Pintos-Morell, R Reisin, K Nicholls, LE Figuera, ... Genetics in Medicine 12 (11), 713-720, 2010 | 55 | 2010 |
| Intron 4 VNTR (4a/b) polymorphism of the endothelial nitric oxide synthase gene is associated with breast cancer in Mexican women R Ramírez-Patiño, LE Figuera, AM Puebla-Pérez, JI Delgado-Saucedo, ... Journal of Korean medical science 28 (11), 1587-1594, 2013 | 46 | 2013 |
| 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 | 41 | 2014 |
| Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRs H Rangel-Villalobos, F Rivas, L Sandoval, B Ibarra, ZY Garcia-Carvajal, ... Human Biology, 983-995, 2000 | 41 | 2000 |
| 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 | 38 | 2009 |
| The Myhre syndrome: report of two cases D Garcia‐Cruz, LE Figuera, A Feria‐Velazco, J Sánchez‐Corona, ... Clinical genetics 44 (4), 203-207, 1993 | 38 | 1993 |
