M. Urioste

发表

Epigenetic differences arise during the lifetime of monozygotic twins.

T. Spector, E. Carlsson, M. Fraga, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Short communication Characterization of the A673 cell line (Ewing tumor) by molecular cytogenetic techniques

M. Urioste, J. Benítez, Á. Martínez-Ramírez, 2003 .

Analysis of myelodysplastic syndromes with complex karyotypes by high‐resolution comparative genomic hybridization and subtelomeric CGH array

J. Cigudosa, M. Urioste, J. Benítez, 2005, Genes, chromosomes & cancer.

Concurrence of germline mutations in the APC and PTEN genes in a colonic polyposis family member.

M. Urioste, J. Benítez, R. Rodríguez-López, 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

M. Urioste, J. Benítez, M. Blasco, 2014, Breast Cancer Research and Treatment.

A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriers

M. Urioste, J. Benítez, A. Osorio, 2006, Human mutation.

RECQL5: Another DNA helicase potentially involved in hereditary breast cancer susceptibility

M. Urioste, J. Benítez, G. Pita, 2019, Human mutation.

A mutation in the POT1 gene is responsible for cardiac angiosarcoma in TP53-negative Li–Fraumeni-like families

F. Setién, M. Urioste, J. Benítez, 2015, Nature Communications.

Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.

M. Urioste, J. Fernández-Piqueras, M. Martinez-frias, 1994, American journal of medical genetics.

Germline missense pathogenic variants in the BRCA1 BRCT domain, p.Gly1706Glu and p.Ala1708Glu, increase cellular sensitivity to PARP inhibitor olaparib by a dominant negative effect.

F. Setién, M. Urioste, J. Benítez, 2016, Human molecular genetics.

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

M. Urioste, P. Chanson, M. Blok, 2012, Clinical Cancer Research.

Analysis of the INK4a/ARF locus in non-Hodgkin’s lymphomas using two new internal microsatellite markers

M. Urioste, J. Benítez, M. Herranz, 1999, Leukemia.

Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement.

N. Carter, J. Cigudosa, M. Urioste, 2004, Human molecular genetics.

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas.

M. Urioste, Giovanni Cianchetta, G. Pita, 2019, American journal of human genetics.

MLH1 germline epimutations in selected patients with early‐onset non‐polyposis colorectal cancer

M. Urioste, J. Benítez, L. Valle, 2007, Clinical genetics.

Concentration and “foreignisation” of land in Bolivia

M. Urioste, 2012 .

Parity and the risk of breast and ovarian cancer in BRCA1 and BRCA2 mutation carriers

M. Urioste, J. Benítez, I. Chirivella, 2009, Breast Cancer Research and Treatment.

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.

Juan F. García, F. Setién, M. Urioste, 2015, Journal of the National Cancer Institute.

The wide spectrum of POT1 gene variants correlates with multiple cancer types

M. Urioste, J. Benítez, C. Lázaro, 2017, European Journal of Human Genetics.

Early-Onset Colorectal Cancer is an Easy and Effective Tool to Identify Retrospectively Lynch Syndrome

M. Urioste, J. Benítez, M. Hidalgo, 2011, Annals of Surgical Oncology.

Approach to early-onset colorectal cancer: clinicopathological, familial, molecular and immunohistochemical characteristics.

M. Urioste, M. Hidalgo, R. González-Sarmiento, 2010, World journal of gastroenterology.

Molecular insights into the OGG1 gene, a cancer risk modifier in BRCA1 and BRCA2 mutations carriers

M. Urioste, J. Benítez, M. Blasco, 2016, Oncotarget.

Commentary: Genomic Analysis Reveals Heterogeneity Between Lesions in Synchronous Primary Right-Sided and Left-Sided Colon Cancer

M. Urioste, R. González-Sarmiento, L. Corchete, 2022, Frontiers in Molecular Biosciences.

Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization

M. Urioste, J. García, D. Rueda, 2017, Clinical colorectal cancer.

Evaluation of the interacting genes and in familial breast cancer susceptibility

M. Urioste, J. Benítez, A. Osorio, 2020 .

Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases

M. Urioste, J. Benítez, P. Pharoah, 2012, Journal of Medical Genetics.

Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene

M. Urioste, J. Benítez, A. Osorio, 2017, Breast Cancer Research and Treatment.

Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes

M. Urioste, J. Benítez, A. Osorio, 2017, British Journal of Cancer.

Cohort profile: the Spanish Early-onset Colorectal Cancer (SECOC) cohort: a multicentre cohort study on the molecular basis of colorectal cancer among young individuals in Spain

N. Malats, M. Urioste, R. González-Sarmiento, 2021, BMJ Open.

Short rib-polydactyly syndrome and pericentric inversion of chromosome 4.

M. Urioste, E. Bermejo, M. Martinez-frias, 1994, American journal of medical genetics.

Chromosome 4p16 and osteochondroplasias

M. Urioste, E. Bermejo, M. Martinez-frias, 1994, Nature Genetics.

Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.

M. Urioste, J. Benítez, A. González-Neira, 2009, American journal of human genetics.

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

M. Urioste, R. Andrés, J. Rosell, 2021, Orphanet Journal of Rare Diseases.

Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

S. Puig, M. Urioste, R. González-Sarmiento, 2018, The British journal of dermatology.

Epidemiological analysis of multi-site closure failure of neural tube in humans.

M. Urioste, E. Bermejo, M. Martinez-frias, 1996, American journal of medical genetics.

Lethal short rib-polydactyly syndromes: further evidence for their overlapping in a continuous spectrum.

M. Urioste, E. Bermejo, M. Martinez-frias, 1993, Journal of medical genetics.

Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia.

M. Urioste, E. Bermejo, M. Martinez-frias, 1994, American journal of medical genetics.

Apparent regional differences in the spectrum of BARD1 pathogenic variants in Spanish population and importance of copy number variants

M. Urioste, A. González-Neira, G. Pita, 2022, Scientific Reports.

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis

A. Valencia, T. Pons, F. Setién, 2018, Molecular Cancer.

Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping.

J. Cigudosa, M. Urioste, J. Benítez, 2004, Cancer genetics and cytogenetics.

Identification of ins(8;21) with AML1/ETO fusion in acute myelogenous leukemia M2 by molecular cytogenetics.

M. Urioste, J. Benítez, Á. Martínez-Ramírez, 2002, Cancer genetics and cytogenetics.

Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1)

J. Cigudosa, M. Urioste, J. Benítez, 2003, Human Genetics.

Surgical management of hereditary colorectal cancer: surgery based on molecular analysis and family history.

M. Urioste, M. Hidalgo, I. Justo, 2009, Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva.

Comment on ‘Wild-type APC prediction of poor prognosis in microsatellite-stable proximal colorectal cancer differs according to the age of onset'

M. Urioste, R. González-Sarmiento, J. García, 2016, British Journal of Cancer.

Mutational analysis of telomere genes in BRCA1/2-negative breast cancer families with very short telomeres

M. Urioste, J. Benítez, A. Osorio, 2012, Breast Cancer Research and Treatment.

Value of clinical analysis in epidemiological research: the Spanish registry experience.

M. Urioste, E. Bermejo, M. Martinez-frias, 1991, American journal of medical genetics.

[Influence of age on the surgical treatment of lynch syndrome].

M. Urioste, M. Hidalgo, J. Perea, 2010, Cirugia espanola.

Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma.

J. Cigudosa, M. Urioste, J. Benítez, 2002, Cancer genetics and cytogenetics.

Biallelic germline mutations in MAD1L1 induce a syndrome of aneuploidy with high tumor susceptibility

M. Urioste, M. Malumbres, S. Rodríguez-Perales, 2022, Science advances.

Bilallelic germline mutations in MAD1L1 induce a novel syndrome of aneuploidy with high tumor susceptibility

M. Urioste, M. Malumbres, S. Rodríguez-Perales, 2022, bioRxiv.

Clinical and functional characterization of the CDH1 germline variant c.1679C>G in three unrelated families with hereditary diffuse gastric cancer

M. Urioste, J. Sanches, R. Seruca, 2018, European Journal of Human Genetics.

Fluorescence in situ hybridization study of TEL/AML1 fusion and other abnormalities involving TEL and AML1 genes. Correlation with cytogenetic findings and prognostic value in children with acute lymphocytic leukemia.

M. Urioste, J. Benítez, Á. Martínez-Ramírez, 2001, Haematologica.

Novel genes and sex differences in COVID-19 severity

Gloria L. Porras-Hurtado, M. Urioste, M. Buti, 2022, Human molecular genetics.

Malignant degeneration of presacral teratoma in the Currarino anomaly

M. Urioste, J. Benítez, L. Valle, 2004, American journal of medical genetics. Part A.

Short rib-polydactyly syndrome (SRPS) with anencephaly and other central nervous system anomalies: a new type of SRPS or a more severe expression of a known SRPS entity?

M. Urioste, E. Bermejo, M. Martínez‐Frías, 1993, American journal of medical genetics.

Anorectal anomalies and Down syndrome.

M. Urioste, M. Martínez‐Frías, 1991, American journal of medical genetics.

Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families

M. Paz, M. Urioste, J. Benítez, 2007, Modern Pathology.

Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies.

M. Urioste, M. Pardo, R. Escribá, 1993, American journal of medical genetics.

Methimazole in animal feed and congenital aplasia cutis

M. Urioste, A. Cereijo, M. Martínez‐Frías, 1992, The Lancet.

Molecular cytogenetic characterization of rhabdomyosarcoma cell lines.

J. Cigudosa, M. Urioste, J. Benítez, 2004, Cancer genetics and cytogenetics.

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance

A. Valencia, T. Pons, M. Urioste, 2015, Genetics in Medicine.

Segmentation anomalies of the vertebras and ribs: a developmental field defect: epidemiologic evidence.

M. Urioste, M. Martínez‐Frías, 1994, American journal of medical genetics.

Epidemiological analysis of the schisis association in the Spanish registry of congenital malformations.

M. Urioste, E. Bermejo, J. Frías, 1997, American journal of medical genetics.

Giant-cell chondrodysplasia in a male infant with clinical and radiological findings resembling the Piepkorn type of lethal osteochondrodysplasia.

M. Urioste, N. Torán, A. Villa, 1997, American journal of medical genetics.

Clinical/epidemiological analysis of congenital anomalies associated with diaphragmatic hernia.

M. Urioste, E. Bermejo, L. Prieto, 1996, American journal of medical genetics.

Pericentric inversions of chromosome 4: report of a new family and review of the literature

M. Urioste, A. Villa, M. Carrascosa, 1995, Clinical Genetics.

Distal deletion of chromosome 13 in a child with the "opitz" GBBB syndrome.

M. Urioste, A. Villa, R. Barrio, 1995, American journal of medical genetics.

Primary midline developmental field. II. Clinical/epidemiological analysis of alteration of laterality (normal body symmetry and asymmetry).

M. Urioste, E. Bermejo, L. Paisán, 1995, American journal of medical genetics.

Ectrodactyly in trisomy 13 syndrome.

M. Urioste, M. Martínez‐Frías, P. Aparicio, 1994, American journal of medical genetics.

De novo interstitial deletion q16.2q21 on chromosome 6.

M. Urioste, A. Villa, J. Bofarull, 1995, American journal of medical genetics.

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.

A. Valencia, T. Pons, M. Urioste, 2018, Gastroenterology.

Erratum: Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis

M. Urioste, R. Valdés-Mas, V. Moreno, 2016, Scientific Reports.

Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis

M. Urioste, X. Puente, V. Moreno, 2016, Scientific Reports.

New case of limb body-wall complex associated with sirenomelia sequence.

M. Urioste, M. Martínez‐Frías, F. Cucalón, 1992, American journal of medical genetics.

Proximal partial 5p trisomy resulting from a maternal (19;5) insertion.

M. Urioste, A. Villa, I. Lorda‐Sánchez, 1997, American journal of medical genetics.

Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.

M. Urioste, A. Diaz de Bustamante, I. Pinel, 1988, American journal of medical genetics.

Anencephaly and limb deficiencies.

M. Urioste, J. Rodríguez-Peralto, J. Palacios, 1992, American journal of medical genetics.

Chromosome cultures from human cartilage.

M. Urioste, 1993, American journal of medical genetics.

Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs.

M. Urioste, M. Martínez‐Frías, A. Arroyo, 1991, American journal of medical genetics.

Anencephaly and faciocranioschisis: evidence of complete failure of closure 3 of the neural tube in humans.

M. Urioste, A. Rosa, 1998, American journal of medical genetics.

A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia

M. Urioste, J. Benítez, M. Robledo, 2013, European Journal of Human Genetics.

Whole exome sequencing identifies PLEC, EXO5 and DNAH7 as novel susceptibility genes in testicular cancer

M. Urioste, J. Benítez, C. López, 2018, International journal of cancer.

Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma.

Joaquín Dopazo, Roger L Milne, Angel Carracedo, 2007, Cancer research.

Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition.

Ana Osorio, Javier Benítez, M. Urioste, 2009, Carcinogenesis.

DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas

M. Urioste, J. Benítez, M. A. van de Wiel, 2013, British Journal of Cancer.

Severe congenital limb deficiencies, vertebral hypersegmentation, absent thymus and mirror polydactyly: A defect expression of a developmental control gene?

M. Urioste, I. Lorda‐Sánchez, E. Burón, 1996, Human Genetics.

Adult acute myeloid leukemia cells do not express nonfunctional Ikaros isoforms

J. Cigudosa, M. Urioste, J. Benítez, 2002 .

MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families.

N. Rosenberg, S. Gruber, M. Urioste, 2010, Cancer research.

Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation.

M. Urioste, J. Benítez, M. Calasanz, 2003, Cancer genetics and cytogenetics.

Cimp-Positive Status is More Representative in Multiple Colorectal Cancers than in Unique Primary Colorectal Cancers

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, Scientific Reports.

Clinical and Molecular Comparative Study of Colorectal Cancer Based on Age-of-Onset and Tumor Location: Two Main Criteria for Subclassifying Colorectal Cancer

M. Urioste, R. González-Sarmiento, L. Inglada-Perez, 2019, International journal of molecular sciences.

Multiple oncogenic mutations and clonal relationship in spatially distinct benign human epidermal tumors

N. Malats, F. Real, J. Cigudosa, 2010, Proceedings of the National Academy of Sciences.

New acrofacial dysostosis syndrome in 3 sibs.

M. Urioste, J. Palacios, J. Rodríguez, 1990, American journal of medical genetics.

Allelic losses and genetic instabilities of PTEN and p73 in non-Hodgkin lymphomas

M. Urioste, J. Benítez, M. Herranz, 2000, Leukemia.

Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.

M. Urioste, J. Benítez, G. Capellá, 2011, Annals of oncology : official journal of the European Society for Medical Oncology.

Fluorescence in situ hybridization study of TEL / AML 1 fusion and other abnormalities involving TEL and AML 1 genes . Correlation with cytogenetic findings and prognostic value in children with acute lymphoblastic leukemia

J. Cigudosa, M. Urioste, C. Soto, 2022 .

Genetic variation in the NEIL2 DNA glycosylase gene is associated with oxidative DNA damage in BRCA2 mutation carriers

Miguel, M. Urioste, J. Benítez, 2017, Oncotarget.

Copy neutral loss of heterozygosity (cnLOH) patterns in synchronous colorectal cancer

M. Urioste, R. González-Sarmiento, L. Corchete, 2020, European Journal of Human Genetics.

Mutations in the DNA mismatch repair gene MLH1 associated with early-onset colon cancer.

M. Urioste, S. Borrego, G. Antiñolo, 2006, The Journal of pediatrics.

Evaluation of the BRCA1 interacting genes RAP80 and CCDC98 in familial breast cancer susceptibility

M. Urioste, J. Benítez, A. Osorio, 2008, Breast Cancer Research and Treatment.

The Average Cumulative Risks of Breast and Ovarian Cancer for Carriers of Mutations in BRCA1 and BRCA2 Attending Genetic Counseling Units in Spain

M. Urioste, J. Benítez, A. Antoniou, 2008, Clinical Cancer Research.

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

Miguel Ángel Martínez, N. Rahman, Pablo I Alarcón, 2019, European Journal of Human Genetics.

Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis

A. Valencia, T. Pons, M. Urioste, 2018, Human mutation.

Anorectal and esophageal anomalies in down syndrome

M. Urioste, A. Cereijo, M. Martínez‐Frías, 1992 .

About the origin and development of hereditary conventional renal cell carcinoma in a four-generation t(3;8)(p14.1;q24.23) family

J. Cigudosa, M. Urioste, J. Benítez, 2005, European Journal of Human Genetics.

Genetic Anticipation Is Associated with Telomere Shortening in Hereditary Breast Cancer

M. Urioste, J. Benítez, A. Osorio, 2011, PLoS genetics.

Germline CDH1 G212E Missense Variant: Combining Clinical, In Vitro and In Vivo Strategies to Unravel Disease Burden

M. Urioste, R. Seruca, Soraia Melo, 2021, Cancers.

A predictor based on the somatic genomic changes of the BRCA1/BRCA2 breast cancer tumors identifies the non-BRCA1/BRCA2 tumors with BRCA1 promoter hypermethylation.

Ana Osorio, Javier Benitez, Ramon Diaz-Uriarte, 2005, Clinical cancer research : an official journal of the American Association for Cancer Research.

Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girl.

M. Urioste, A. Villa, I. Lorda‐Sánchez, 1997, American journal of medical genetics.

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.

A. Valencia, T. Pons, M. Urioste, 2015, Gastroenterology.

Lhermitte-Duclos disease and Cowden disease: clinical and genetic study in five patients with Lhermitte-Duclos disease and literature review

M. Urioste, J. Benítez, A. Lagares, 2004, Acta Neurochirurgica.

Clinical Article Lhermitte-Duclos disease and Cowden disease: clinical and genetic study in five patients with Lhermitte-Duclos disease and literature review

M. Urioste, A. Lagares, R. Lobato, 2004 .

Genetic characterization and structural analysis of VHL Spanish families to define genotype–phenotype correlations

M. Urioste, J. Benítez, A. Cebrián, 2004, Human mutation.

Investigation on the Role of PALB2 Gene in CDH1-Negative Patients With Hereditary Diffuse Gastric Cancer

M. Urioste, M. Carreño, J. Perea, 2020, Clinical and translational gastroenterology.

The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

B. Bonanni, M. Urioste, J. Benítez, 2020, Cancers.

Deletion at 6q24.2–26 predicts longer survival of high‐grade serous epithelial ovarian cancer patients

J. Cigudosa, M. Urioste, J. Benítez, 2014, Molecular oncology.

De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19

J. Cigudosa, M. Urioste, J. Benítez, 2003, Genes, chromosomes & cancer.

Intermediate-onset colorectal cancer: A clinical and familial boundary between both early and late-onset colorectal cancer

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, PloS one.

Age at onset should be a major criterion for subclassification of colorectal cancer.

M. Urioste, J. Benítez, D. Rueda, 2014, The Journal of molecular diagnostics : JMD.

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

M. Urioste, J. Benítez, J. Hernández, 2016, Molecular carcinogenesis.

Cytogenetic characterization reveals that the SAM-1 erythroid cell line is derived from K-562 cells.

J. Cigudosa, M. Urioste, J. Benítez, 2002, Blood.

Acrofacial dysostosis syndromes.

M. Urioste, J. Palacios, J. Rodríguez, 1992, American journal of medical genetics.

Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas

M. Urioste, J. Benítez, B. Martínez-Delgado, 2001, Leukemia.

NOMO-1 gene is deleted in early-onset colorectal cancer

M. Urioste, R. González-Sarmiento, J. García, 2017, Oncotarget.

Bolivia: Reform and Resistance in the Countryside (1982-2000)

M. Urioste, 2001 .

Land market in a new context: the INRA law in Bolivia.

M. Urioste, D. Pacheco, 2000 .

Tetra-phocomelia with multiple malformations: X-linked amelia, or Roberts syndrome, or DK-phocomelia syndrome?

M. Urioste, J. Rodríguez-Peralto, J. Palacios, 1992, American journal of medical genetics.

DK-phocomelia syndrome in a child with a long follow-up.

M. Urioste, L. Paisán, M. Martínez‐Frías, 1994, American journal of medical genetics.

An unusual variant of chromosome 16

M. Urioste, V. Félix, A. Diaz de Bustamante, 1988, Human Genetics.

DNA repair capacity is impaired in healthy BRCA1 heterozygous mutation carriers

F. Setién, M. Urioste, J. Benítez, 2015, Breast Cancer Research and Treatment.

Clinicopathologic and pedigree differences in amsterdam I-positive hereditary nonpolyposis colorectal cancer families according to tumor microsatellite instability status.

M. Urioste, J. Benítez, L. Valle, 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Retrorectal cystic hamartoma as benign cause of CA 19-9 elevation.

M. Urioste, J. García-Donas, C. Jara, 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Human Cancer Biology MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

M. Urioste, P. Chanson, M. Blok, 2012 .

Genome-wide linkage analysis and tumoral characterization reveal heterogeneity in familial colorectal cancer type X

M. Urioste, A. González-Neira, G. Pita, 2015, Journal of Gastroenterology.

Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families

M. Urioste, J. Benítez, C. Lázaro, 2009, Breast Cancer Research and Treatment.

Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments.

M. Urioste, E. Guinó, G. Capellá, 2008, Clinical chemistry.

Redefining synchronous colorectal cancers based on tumor clonality

M. Urioste, L. Corchete, D. García-Olmo, 2018, International journal of cancer.

MOLECULAR CLASSIFICATION OF SYNCHRONOUS COLORECTAL CANCER : CLINICAL AND MOLECULAR CHARACTERIZATION Running title : Characterization of synchronous colorectal cancer

M. Urioste, J. García, D. Rueda, 2016 .

Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes1

M. Urioste, R. González-Sarmiento, J. García, 2016, Neoplasia.

POT1 and Damage Response Malfunction Trigger Acquisition of Somatic Activating Mutations in the VEGF Pathway in Cardiac Angiosarcomas

M. Urioste, J. Benítez, C. Lázaro, 2019, Journal of the American Heart Association.

Functional analysis of PTEN variants of unknown significance from PHTS patients unveils complex patterns of PTEN biological activity in disease

M. Urioste, V. J. Cid, M. Molina, 2022, European Journal of Human Genetics.

Response to Dr. Hecht

M. Urioste, J. I. Rodríguez, J. Palacios, 1992 .

Clinical and functional characterization of the CDH1 germline variant c.1679C>G in three unrelated families with hereditary diffuse gastric cancer

M. Urioste, J. Sanches, R. Seruca, 2018, European Journal of Human Genetics.

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore.

M. Urioste, J. Benítez, R. González-Sarmiento, 2015, American journal of cancer research.

Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Matthew A. Wiles, Ellen C. Smith, Jack D. Sanders, 2023, Nature.

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Matthew A. Wiles, Ellen C. Smith, Jack D. Sanders, 2023, Nature.

A new case of fibrochondrogenesis from Spain.

M. Urioste, J. Rodríguez, J. Cuevas, 1996, Journal of medical genetics.

Differential clinicopathological and molecular features within late-onset colorectal cancer according to tumor location

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2018, Oncotarget.

Frequency and impact of KRAS mutation in early onset colorectal cancer.

M. Urioste, R. González-Sarmiento, J. García, 2017, Human pathology.

Cimp-Positive Status is More Representative in Multiple Colorectal Cancers than in Unique Primary Colorectal Cancers

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, Scientific Reports.

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas.

M. Urioste, Giovanni Cianchetta, G. Pita, 2019, American journal of human genetics.

Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2019, Cancers.

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.

Juan F. García, F. Setién, M. Urioste, 2015, Journal of the National Cancer Institute.

The average cumulative risks of breast and ovarian cancer for carriers of mutations in BRCA1 and BRCA2 attending genetic counseling units in Spain.

M. Urioste, J. Benítez, A. Antoniou, 2008, Clinical Cancer Research.

Age at onset should be a major criterion for subclassification of colorectal cancer.

M. Urioste, J. Benítez, D. Rueda, 2014, The Journal of molecular diagnostics : JMD.

Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

M. Urioste, A. Osorio, L. Inglada-Perez, 2014, Breast Cancer Research and Treatment.

MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families.

N. Rosenberg, S. Gruber, M. Urioste, 2010, Cancer research.

From The Cover : Epigenetic differences arise during the lifetime of monozygotic twins

T. Spector, E. Carlsson, M. Fraga, 2005 .

A clinico-pathological and molecular analysis reveals differences between solitary (early and late-onset) and synchronous rectal cancer

M. Urioste, R. González-Sarmiento, L. Corchete, 2021, Scientific Reports.

Comment on ‘Distinct clinical outcomes of two CIMP-positive colorectal cancer subtypes based on a revised CIMP classification system’

M. Urioste, R. González-Sarmiento, D. García-Olmo, 2018, British Journal of Cancer.

A second update on mapping the human genetic architecture of COVID-19

M. A. Hakim Newton, Jack D. Sanders, Jonathan H. Morgan, 2022, Nature.

Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.

M. Urioste, J. Benítez, A. González-Neira, 2009, American journal of human genetics.

A common SNP in the UNG gene decreases ovarian cancer risk in BRCA2 mutation carriers

M. Urioste, J. Benítez, A. Osorio, 2019, Molecular oncology.