I P Davalos

Summary

Publications

  1. ncbi request reprint Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome
    L E Figuera
    Division de Genetica, CIBO, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico
    Clin Dysmorphol 11:243-7. 2002
  2. ncbi request reprint Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia
    I P Davalos
    Divisiones de Genética y Medicina Molecular del Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Sierra Mojada 800, Col Independencia, CMNO, CP 44330, Guadalajara, Jal Mexico
    Blood Cells Mol Dis 35:66-9. 2005
  3. ncbi request reprint Zimmermann-Laband syndrome: further clinical delineation
    I P Davalos
    Divisiones de Genética, CIBO, CMNO, IMSS, Guadalajara, Jalisco, Mexico
    Genet Couns 16:283-90. 2005
  4. pmc MTHFR C677T, MTHFR A1298C, and OPG A163G polymorphisms in Mexican patients with rheumatoid arthritis and osteoporosis
    Aniel Jessica Leticia Brambila-Tapia
    Doctorado en Genetica Humana, Instituto de Genetica Humana, CUCS, Universidad de Guadalajara and División de Genética, CIBO, Instituto Mexicano del Seguro Social IMSS, Jalisco, Mexico
    Dis Markers 32:109-14. 2012
  5. ncbi request reprint Wide clinical spectrum in Zimmermann-Laband syndrome
    I P Davalos
    Division de Genetica, Centro de lnvestigación Biomédica de Occidente, Instituto Mexicano del Seguro Social IMSS, Guadalajara, Jalisco, Mexico
    Genet Couns 22:1-10. 2011
  6. ncbi request reprint [Non-syndromic cleft lip/cleft palate and C677T methylene-tetrahydrofolate reductase variant in Mexican children]
    Ingrid Patricia Dávalos-Rodríguez
    Centro de Investigacion Biomedica de Occidente, Universidad de Guadalajara, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico
    Rev Med Inst Mex Seguro Soc 47:549-52. 2009
  7. ncbi request reprint A variant example of familial Floating-Harbor syndrome?
    J M Peñaloza
    Divisiones de Genética, Centro de Investigacion Biomedica de Occidente, CMNO, IMSS, Guadalajara, Jalisco, Mexico
    Genet Couns 14:31-7. 2003
  8. doi request reprint Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases
    J P Mena
    Doctorado en Genetica Humana, Instituto de Genetica Humana, Centro Universitario Ciencias de la Salud CUCS, Universidad de Guadalajara U de G, Guadalajara, Mexico
    Pharmacogenomics J 11:287-91. 2011
  9. ncbi request reprint A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp
    N O Davalos
    Instituto de Genetica Humana Dr Enrique Corona Rivera, CUCS, Universidad de Guadalajara, Guadalajara, Mexico
    Br J Dermatol 153:1216-9. 2005
  10. ncbi request reprint Reproductive history in mothers of children with neural tube defects
    F Rivas
    Division de Genetica, Centro de Investigacion Biomedica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico
    Gynecol Obstet Invest 49:255-60. 2000

Collaborators

  • X Xu
  • R Kruse
  • R C Betz
  • L E Figuera
  • F Rivas
  • S E Flores Martinez
  • Aniel Jessica Leticia Brambila-Tapia
  • N O Davalos
  • A I Vásquez-Velásquez
  • J P Mena
  • Mario Salazar-Paramo
  • Valeria Peralta-Leal
  • Juan Pablo Mena
  • Jorge Duran-Gonzalez
  • Ingrid Patricia Dávalos-Rodríguez
  • D Garcia-Cruz
  • J M Peñaloza
  • Laura Gonzalez-Lopez
  • Monica Vazquez Del Mercado
  • Lucila Sandoval-Ramirez
  • Claudia Patricia Beltrán-Miranda
  • Brissia Lazalde-Medina B
  • Nory Omayra Dávalos
  • Jorge Iván Gámez-Nava
  • F J Muñoz-Valle
  • M Salazar-Paramo
  • H Rivera
  • L Gonzalez-Lopez
  • M G González-Mercado
  • G Raca
  • J D Sanchez
  • H A García-Castillo
  • E Dwyer
  • M Vazquez Del Mercado
  • J I Gamez-Nava
  • L Sandoval-Ramirez
  • Víctor Ledezma-Rodríguez
  • Ernesto Javier Ramírez-Lizardo
  • Mirna Gisel González-Mercado
  • María Cristina Morán-Moguel
  • Nory Omayra-Dávalos
  • Víctor Ledezma-Gómez
  • A García-Vargas
  • V J Picos-Cárdenas
  • M M Nöthen
  • J Pforr
  • J Sanchez-Corona
  • M O Garcia-Cruz
  • D Perez-Rulfo

Detail Information

Publications11

  1. ncbi request reprint Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome
    L E Figuera
    Division de Genetica, CIBO, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico
    Clin Dysmorphol 11:243-7. 2002
    ..The authors propose this as a new entity, and have designated it Guadalajara camptodactyly type III...
  2. ncbi request reprint Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia
    I P Davalos
    Divisiones de Genética y Medicina Molecular del Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Sierra Mojada 800, Col Independencia, CMNO, CP 44330, Guadalajara, Jal Mexico
    Blood Cells Mol Dis 35:66-9. 2005
    ..We conclude that these polymorphisms do not contribute in the etiology of PE/E as it has been reported in other populations...
  3. ncbi request reprint Zimmermann-Laband syndrome: further clinical delineation
    I P Davalos
    Divisiones de Genética, CIBO, CMNO, IMSS, Guadalajara, Jalisco, Mexico
    Genet Couns 16:283-90. 2005
    ..A wide clinical spectrum in ZLS is also considered...
  4. pmc MTHFR C677T, MTHFR A1298C, and OPG A163G polymorphisms in Mexican patients with rheumatoid arthritis and osteoporosis
    Aniel Jessica Leticia Brambila-Tapia
    Doctorado en Genetica Humana, Instituto de Genetica Humana, CUCS, Universidad de Guadalajara and División de Genética, CIBO, Instituto Mexicano del Seguro Social IMSS, Jalisco, Mexico
    Dis Markers 32:109-14. 2012
    ....
  5. ncbi request reprint Wide clinical spectrum in Zimmermann-Laband syndrome
    I P Davalos
    Division de Genetica, Centro de lnvestigación Biomédica de Occidente, Instituto Mexicano del Seguro Social IMSS, Guadalajara, Jalisco, Mexico
    Genet Couns 22:1-10. 2011
    ..We suggest that this case supports that ZLS can be part a contiguous genes syndrome or be consequence ofa gene mutation with wide variable expression. The present report supports that ZLS has a wide clinical spectrum...
  6. ncbi request reprint [Non-syndromic cleft lip/cleft palate and C677T methylene-tetrahydrofolate reductase variant in Mexican children]
    Ingrid Patricia Dávalos-Rodríguez
    Centro de Investigacion Biomedica de Occidente, Universidad de Guadalajara, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico
    Rev Med Inst Mex Seguro Soc 47:549-52. 2009
    ..Our objective was to determine the allelic (AF) and genotypic frequency (GF) of the MTHFR-C677T variant in Mexican children with NSCLP...
  7. ncbi request reprint A variant example of familial Floating-Harbor syndrome?
    J M Peñaloza
    Divisiones de Genética, Centro de Investigacion Biomedica de Occidente, CMNO, IMSS, Guadalajara, Jalisco, Mexico
    Genet Couns 14:31-7. 2003
    ..His mother also presents minor phenotypical characteristics, suggesting that the present observation corresponds to a variant example of familial FHS...
  8. doi request reprint Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases
    J P Mena
    Doctorado en Genetica Humana, Instituto de Genetica Humana, Centro Universitario Ciencias de la Salud CUCS, Universidad de Guadalajara U de G, Guadalajara, Mexico
    Pharmacogenomics J 11:287-91. 2011
    ..024). The identification of MTHFR genotypes for C677T and A1298C polymorphisms could lead clinicians to identify patients in risk of elevation of transaminases, and give them an individualized treatment, as is a goal of pharmacogenetics...
  9. ncbi request reprint A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp
    N O Davalos
    Instituto de Genetica Humana Dr Enrique Corona Rivera, CUCS, Universidad de Guadalajara, Guadalajara, Mexico
    Br J Dermatol 153:1216-9. 2005
    ..3), allowing mutations in the corneodesmosin gene (CDSN) to be identified as the cause of the disorder. To date, two stop mutations have been found in three unrelated families with HSS of different ethnic origin...
  10. ncbi request reprint Reproductive history in mothers of children with neural tube defects
    F Rivas
    Division de Genetica, Centro de Investigacion Biomedica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico
    Gynecol Obstet Invest 49:255-60. 2000
    ..05). An increased number of abortions adjacent to affected offspring and a changing fertility pattern, depending on the product diagnosis, point to an environmental etiological component in this high-risk NTD group of mothers...
  11. doi request reprint Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism
    A I Vásquez-Velásquez
    Division de Genetica, CIBO, Instituto Mexicano del Seguro Social, Guadalajara, Mexico
    Cytogenet Genome Res 132:233-8. 2011
    ....