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Employment (3)

Hospital Universitario La Paz: Madrid, Madrid, ES

2015-11-10 to present (Instituto de Genética Médica y Molecular INGEMM)
Employment
Source: Self-asserted source
Isabel Vallcorba

Hospital Universitario Infanta Cristina: Badajoz, Extremadura, ES

2006-09-01 to 2015-11-09 (Inmunología y Genética)
Employment
Source: Self-asserted source
Isabel Vallcorba

Hospital Universitario La Paz: Madrid, Madrid, ES

2004-11-01 to 2006-08-31 (Genética)
Employment
Source: Self-asserted source
Isabel Vallcorba

Education and qualifications (2)

Universidad de Alcalá de Henares Facultad de Medicina y Ciencias de la Salud: Alcala de Henares, Madrid, ES

2005-01-13 to present | Doctorado
Education
Source: Self-asserted source
Isabel Vallcorba

Universidad Complutense de Madrid: Madrid, Comunidad de Madrid, ES

1987-03-13 to present | Lda Ciencias Biológicas
Education
Source: Self-asserted source
Isabel Vallcorba

Works (22)

Mortality in Patients with 22q11.2 Rearrangements

Genes
2024-08 | Journal article | Author
DOI: 10.3390/genes15091146
Contributors: Melisa Cilio Arroyuelo; Jair Antonio Tenorio; Luis Fernandez; Alejandro Parra; Mario Cazalla Garcia; Natalia Gallego ; Lucía Miranda-Alcaraz; María Ángeles Mori; Luis García-Gueretta; Carlos Labrandero de Lera et al.
Source: check_circle
Multidisciplinary Digital Publishing Institute

Memory T Cells Expressing an NKG2D-CAR Efficiently Target Osteosarcoma Cells.

Clinical cancer research : an official journal of the American Association for Cancer Research
2017-10 | Journal article
DOI: 10.1158/1078-0432.ccr-17-0075
PMID: 28659311
Contributors: Fernández L; Metais JY; Escudero A; Vela M; Valentín J; Vallcorba I; Leivas A; Torres J; Valeri A; Patiño-García A et al.
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Celiac disease and HLA-DQ genotype: diagnosis of different genetic risk profiles related to the age in Badajoz, southwestern Spain.

Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva
2013-09 | Journal article
DOI: 10.4321/s1130-01082013000800005
PMID: 24274444
Contributors: Fernández-Cavada-Pollo MJ; Alcalá-Peña MI; Vargas-Pérez ML; Vergara-Prieto E; Vallcorba-Gómez-Del Valle I; Melero-Ruiz J; Márquez-Armenteros AM; González-Roiz C
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: does -7/7q- detection by FISH have prognostic value?

Leukemia research
2013-04 | Journal article
DOI: 10.1016/j.leukres.2012.12.010
PMID: 23337401
Contributors: Ademà V; Hernández JM; Abáigar M; Lumbreras E; Such E; Calull A; Dominguez E; Arenillas L; Mallo M; Cervera J et al.
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

El documento de consentimiento informado para la realización de pruebas genéticas en el ámbito asistencial y en proyectos de investigación

Diagnóstico Prenatal
2013-04 | Journal article
DOI: 10.1016/j.diapre.2012.05.001
Part of ISSN: 2173-4127
Contributors: Teresa Pampols; Joaquín Rueda; Montserrat Milà; Diana Valverde; Nagore Garín; Isabel Vallcorba; Jordi Rosell
Source: Self-asserted source
Isabel Vallcorba via Crossref Metadata Search

Euchromatic variant 16p+. Implications in prenatal diagnosis.

Prenatal diagnosis
2006-06 | Journal article
DOI: 10.1002/pd.1454
PMID: 16634122
Contributors: López Pajares I; Villa O; Salido M; Mori MA; Gonzalez A; Lapunzina P; De Torres ML; Vallcorba I; Palomares M; Fernández L et al.
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

[Hereditary hemochromatosis: phenotypic study in a Spanish population].

Medicina clinica
2005-11 | Journal article
DOI: 10.1016/s0025-7753(05)72169-2
PMID: 16324464
Contributors: Vázquez-Romero M; Boixeda-de Miquel D; Vallcorba-Gómez del Valle I; Foruny-Olcina JR; Martín de Argila C; San Román-Cos-Gayón C
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

[Familiar penetrancy of HFE gene: four brothers of the same family affected by hereditary haemochromatosis].

Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva
2005-08 | Journal article
DOI: 10.4321/s1130-01082005000800014
PMID: 16266232
Contributors: Vázquez Romero M; Boixeda de Miquel D; Martín de Argila de Prados C; Vallcorba Gómez del Valle I; Cabello Albendea P; López San Román A; San Román Cos-Gayón C
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Chromosome 21 tandem repetition and AML1 (RUNX1) gene amplification.

Cancer genetics and cytogenetics
2004-02 | Journal article
DOI: 10.1016/s0165-4608(03)00259-0
PMID: 15104277
Contributors: Ferro MT; Hernaez R; Sordo MT; Garcia-Sagredo JM; Garcia-Miguel P; Fernández Guijarro M; Lopez J; Villalón C; Vallcorba I; Cabello P et al.
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

[Primary hemochromatosis with abnormally low serum ferritin].

Gastroenterologia y hepatologia
2003 | Journal article
PMID: 12809577
Contributors: Vázquez Romero M; Boixeda de Miquel D; Vallcorba Gómez del Valle I; Foruny Olcina JR; Valer López-Fando MP; San Román Cos-Gayón C
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Chromosome 9 interstitial deletion in multiple myeloma.

Cancer genetics and cytogenetics
2002-11 | Journal article
DOI: 10.1016/s0165-4608(02)00625-8
PMID: 12547169
Contributors: Ferro MT; Hernaez R; Villalon C; Sordo MT; Garcia-Sagredo JM; Vallcorba I; Roman CS; Lopez J
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Deletion of the long arm of the Y chromosome in an adolescent with short stature and hypogonadism.

Journal of pediatric endocrinology & metabolism : JPEM
2001-01 | Journal article
DOI: 10.1515/jpem.2001.14.1.103
PMID: 11220698
Contributors: Botella-Carretero JI; Valero MA; Valcorba I; Ezquieta B; Alonso M; Barrio R
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

[The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].

Revista clinica espanola
1999-10 | Journal article
PMID: 10589245
Contributors: Moreno L; Vallcorba P; Boixeda D; Cabello P; Bermejo F; San Román C
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Translocation (9;22;21) in a chronic myeloid leukemia fluorescence in situ hybridization definition.

Cancer genetics and cytogenetics
1998-07 | Journal article
DOI: 10.1016/s0165-4608(97)00413-5
PMID: 9648564
Contributors: Vallcorba I; García-Sagredo JM; San Román C; Ferro MT; González A; Cabello P; Villegas A
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Automated FISH spot counting in interphase nuclei: statistical validation and data correction.

Cytometry
1998-02 | Journal article
DOI: 10.1002/(sici)1097-0320(19980201)31:2<93::aid-cyto4>3.0.co;2-j
PMID: 9482278
Contributors: Ortiz de Solórzano C; Santos A; Vallcorba I; García-Sagredo JM; del Pozo F
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

P XIV C.4 Analysis of mutagenic effect of low frequency electromagnetic fields by chromosome painting

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis
1997-09 | Journal article
DOI: 10.1016/s0027-5107(97)83089-8
Part of ISSN: 0027-5107
Contributors: Jose M. Garcia-Sagredo; Concepcion Villalon; Isabel Vallcorba; Carmen Sanchez-Hombre; Teresa Ferro; Carlos San Roman
Source: Self-asserted source
Isabel Vallcorba via Crossref Metadata Search

Applying watershed algorithms to the segmentation of clustered nuclei.

Cytometry
1997-08 | Journal article
DOI: 10.1002/(sici)1097-0320(19970801)28:4<289::aid-cyto3>3.0.co;2-7
PMID: 9266748
Contributors: Malpica N; de Solórzano CO; Vaquero JJ; Santos A; Vallcorba I; García-Sagredo JM; del Pozo F
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.

American journal of medical genetics
1997-02 | Journal article
DOI: 10.1002/(sici)1096-8628(19970211)68:4<428::aid-ajmg11>3.3.co;2-p
PMID: 9021016
Contributors: Rizzu P; Haddad BR; Vallcorba I; Alonso A; Ferro MT; Garcia-Sagredo JM; Baldini A
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.

Annales de genetique
1996 | Journal article
PMID: 8766134
Contributors: Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Cytogenetic study of neuroendocrine carcinoma of Merkel cells.

Cancer genetics and cytogenetics
1996-11 | Journal article
DOI: 10.1016/0165-4608(94)00189-8
PMID: 8956877
Contributors: Vázquez-Mazariego Y; Vallcorba I; Ferro MT; López-Yarto A; García-Sagredo JM; Cabello P; Resino M; Muñoz R; Mayayo M; San Román C
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Chromosome painting in biological dosimetry: assessment of the ability to score stable chromosome aberrations using different pairs of paint probes.

Environmental health perspectives
1996-05 | Journal article
DOI: 10.2307/3432807
PMID: 8781367
PMC: PMC1469613
Contributors: García Sagredo JM; Vallcorba I; López-Yarto; Sanchez-Hombre MD; Resino M; Ferro MT
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central

Burkitt lymphoma with a duplication of der(8)t(2;8). Interpretation of a complex karyotype by chromosome painting.

Cancer genetics and cytogenetics
1994-09 | Journal article
DOI: 10.1016/0165-4608(94)90464-2
PMID: 7923063
Contributors: Vázquez-Mazariego Y; Cabello P; García-Sagredo JM; López-Yarto A; Vallcorba I; Resino M; Muñoz R; Pérez I; Mayayo M; Ferro MT
Source: Self-asserted source
Isabel Vallcorba via Europe PubMed Central
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