Publications

MARÍA ASUNCIÓN ORERA CLEMENTE publications

22 results

2025

  1. Boosted Genomic Literacy in Nursing Students via Standardized-Patient Clinical Simulation: A Mixed-Methods Study

    Nursing Reports, Vol. 15, Núm. 8

2022

  1. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients

    Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1

  2. Response to anakinra in new-onset refractory status epilepticus: A clinical case

    Seizure, Vol. 94, pp. 92-94

2020

  1. A collection of three integration-free iPSCs derived from old male and female healthy subjects

    Stem Cell Research, Vol. 42

2019

  1. A collection of four integration-free iPSC lines derived from diagnosed sporadic Alzheimer's disease patients with different APOE alleles

    Stem Cell Research, Vol. 39

  2. A collection of integration-free iPSCs derived from Parkinson's disease patients carrying mutations in the GBA1 gene

    Stem Cell Research, Vol. 38

  3. An integration-free iPSC line, ICCSICi007-A, derived from a female Alzheimer's disease patient with the APOE-ε4/ε4 alleles

    Stem Cell Research, Vol. 41

  4. Generation of an integration-free iPSC line, ICCSICi005-A, derived from a Parkinson's disease patient carrying the L444P mutation in the GBA1 gene

    Stem Cell Research, Vol. 40

  5. Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation

    Stem Cell Research, Vol. 40

2015

  1. PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome

    European Journal of Human Genetics, Vol. 23, Núm. 12, pp. 1615-1626

2011

  1. NID2 and HOXA9 promoter hypermethylation as biomarkers for prevention and early detection in oral cavity squamous cell carcinoma tissues and saliva

    Cancer Prevention Research, Vol. 4, Núm. 7, pp. 1061-1072

2009

  1. Quantitative abnormalities of peripheral blood distinct T, B, and natural killer cell subsets and clinical findings in obstetric antiphospholipid syndrome

    Journal of Rheumatology, Vol. 36, Núm. 6, pp. 1217-1225

2007

  1. Monitorización inmunológica en mujeres con aborto recurrente

    Clinica e Investigacion en Ginecologia y Obstetricia, Vol. 34, Núm. 6, pp. 220-223

2004

  1. A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidum

    Prenatal Diagnosis, Vol. 24, Núm. 8, pp. 635-637

  2. An excess of chromosome 1 breakpoints in male infertility

    European Journal of Human Genetics, Vol. 12, Núm. 12, pp. 993-1000

2003

  1. Antiphospholipid syndrome updating

    Medicina Clinica, Vol. 121, Núm. 12, pp. 459-471

2002

  1. La farmacogenética, un nuevo reto

    Farmacia Hospitalaria

2001

  1. Familial Pitt-Rogers-Danks: Two new cases

    Revista de Neurologia, Vol. 33, Núm. 5, pp. 439-443

  2. Molecular analysis of a gestation consisting of a complete hydatidiform mole and normal dizygotic twin

    Journal of Reproductive Medicine for the Obstetrician and Gynecologist, Vol. 46, Núm. 12, pp. 1041-1045

2000

  1. Polydactyly in 22q11 syndrome: Should it be taken into account?

    Clinical Genetics