Author

Félix Prieto

Observed names: FELIX PRIETO, Felix Prieto

Institution: Hospital Universitari i Politècnic La Fe

Observed institutions: Brigham and Women's Hospital, Roswell Park Comprehensive Cancer Center, Lurie Children's Hospital, Howard Hughes Medical Institute, Consejo Superior de Investigaciones Científicas, Harvard University, Universitat de València, University of the Witwatersrand, Universität Ulm, Harrisburg Hospital, Hospital Universitari i Politècnic La Fe, Massachusetts General Hospital

OpenAlex ID: A5113485711

Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF)

2003 · Montserrat Rodríguez-Ballesteros, Francisco J. del Castillo, et al. · Human Mutation · 202

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Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

1997 · Sylvia Bort, E. Nelis, et al. · Human Genetics · 139

Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis

1993 · Francisco Palau, Ann Löfgren, et al. · Human Molecular Genetics · 128

Genetic Heterogeneity of Heart-Hand Syndromes

1995 · Craig T. Basson, Scott D. Solomon, et al. · Circulation · 79

Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma

2006 · Francisco Sánchez-Sánchez, Carmen Ramírez-Castillejo, et al. · Human Mutation · 48

11q23 abnormalities in children with acute nonlymphocytic leukemia (M4–M5)

1990 · Félix Prieto, Francisco Palau, et al. · Cancer Genetics and Cytogenetics · 39

Chromosome 11 Abnormalities in Myelodysplastic Syndromes

1999 · Rosa Collado, Lourdes Badı́a, et al. · Cancer Genetics and Cytogenetics · 38

Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa

1994 · Gunnar Grüning, José M. Millan, et al. · Human Mutation · 36

A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation

2006 · Isabel Martínez-Garay, Miguel Tomás, et al. · European Journal of Human Genetics · 34

Chromosome banding patterns in patients with chronic myelocytic leukemia

1982 · Felix Carbonell, Javier Benitez, et al. · Cancer Genetics and Cytogenetics · 28

Translocations involving chromosomes #3 and #12: Hematologic diseases associated with abnormalities of these chromosomes

1982 · Avery A. Sandberg, Barbara K. Hecht, et al. · Cancer Genetics and Cytogenetics · 28

Pediatric Brain Tumors: Loss of Heterozygosity at 17p and TP53 Gene Mutations

1998 · Carmen Orellana, Miguel Hernandez-Martı́, et al. · Cancer Genetics and Cytogenetics · 27

Trisomy 4: Another specific anomaly in acute nonlymphocytic leukemia

1987 · Felix Prieto, Lourdes Badía, et al. · Cancer Genetics and Cytogenetics · 24

Translocation (11;22) in Ewing's sarcoma

1985 · Felix Prieto, Lourdes Badía, et al. · Cancer Genetics and Cytogenetics · 24

Identification of the Philadelphia (Ph-1) Chromosome

1970 · FELIX PRIETO, JOSE EGOZCUE, et al. · Blood · 23

X-Linked Anhidrotic (Hypohidrotic) Ectodermal Dysplasia Caused by a Novel Mutation in EDA1 Gene: 406T>G (Leu55Arg)

1999 · Francisco Martínez, José María Millán, et al. · Journal of Investigative Dermatology · 21

Genetics of retinoblastoma: A study

1997 · Emilia Mateu, Francisco Sánchez, et al. · Cancer Genetics and Cytogenetics · 21

Gene localization in a family with X‐linked syndromal mental retardation (Prieto syndrome)

1991 · Anke Watty, Félix Prieto, et al. · American Journal of Medical Genetics · 20

Localization of a gene for X‐linked nonspecific mental retardation (MRX24) in Xp22.2–p22.3

1995 · Francisco Martínez, Andreas Gal, et al. · American Journal of Medical Genetics · 17

Cytogenetic studies in 18 patients with secondary blood disorders

1986 · Javier Benitez, Felix Carbonell, et al. · Cancer Genetics and Cytogenetics · 17

Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain

1999 · José M. Millán, Francisco Martínez, et al. · Clinical Genetics · 12

Acute nonlymphoblastic leukemia in children treated for acute lymphoblastic leukemia with an intensive regimen including teniposide

1992 · Amparo Verdeguer, Jose Gabriel Ruiz, et al. · Medical and Pediatric Oncology · 12

Trisomy of the long arm of chromosome 1 in patients with hematologic malignancies and solid tumors: Report of six cases

1988 · Francisco Cervantes, Félix Prieto, et al. · Cancer Genetics and Cytogenetics · 12

A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus

1996 · Patricia Smeyers, Eugènia Monrós, et al. · Human Genetics · 11

A Novel TP53 Germ-Line Mutation Identified in a Girl with a Primitive Neuroectodermal Tumor and Her Father

1998 · Carmen Orellana, Francisco Martı́nez, et al. · Cancer Genetics and Cytogenetics · 10

Works count: 44

Citation count: 1,139

H-index: 18

I10-index: 28