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López‐Fernández, Adrià
74  Ergebnisse:
Personensuche X
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1

Role of psychological background in cancer susceptibility g..:

López‐Fernández, Adrià ; Villacampa, Guillermo ; Salinas, Mònica...
Journal of Genetic Counseling.  32 (2023)  4 - p. 778-787 , 2023
Link: https://doi.org/10.1002/..
 
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2

Opportunistic testing of BRCA1, BRCA2 and mismatch repair g..:

Feliubadaló, Lídia ; López‐Fernández, Adrià ; Pineda, Marta...
International Journal of Cancer.  145 (2019)  10 - p. 2682-2691 , 2019
Link: https://doi.org/10.1002/..
 
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3

Genetic and clinical characterization of a novel FH founder..:

Sánchez-Heras, Ana Beatriz ; Dámaso, Estela ; Castillejo, Adela...
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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4

Co-occurrence of mutations in NF1 and other susceptibility ..:

Mellid, Sara ; Gil, Eduardo ; Letón, Rocío...
Frontiers in Endocrinology.  13 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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5

Mo1151 COLORECTAL ADENOMA PREVALENCE AND INCIDENCE IN LYNCH..:

Sanchez, Ariadna ; Castillo, Joaquin ; Roos, Victorine...
Gastroenterology.  164 (2023)  6 - p. S-776 , 2023
Link: https://doi.org/10.1016/..
 
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6

Mo1154 IS GASTRIC CANCER SCREENING NECESSARY IN LYNCH SYNDR..:

Sanchez, Ariadna ; Arango, Andres ; Moreta, Maria Jose...
Gastroenterology.  164 (2023)  6 - p. S-777-S-778 , 2023
Link: https://doi.org/10.1016/..
 
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7

Author Correction: The Molecular Tumor Board Portal support..:

Tamborero, David ; Dienstmann, Rodrigo ; Rachid, Maan Haj...
Nature Cancer.  3 (2022)  5 - p. 649-649 , 2022
Link: https://doi.org/10.1038/..
 
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8

A case of Rothmund-Thomson syndrome originally thought to b..:

Marmolejo Castañeda, David Humberto ; Cruellas Lapeña, Mara ; Carrasco López, Estela...
Familial Cancer.  22 (2022)  1 - p. 99-102 , 2022
Link: https://doi.org/10.1007/..
 
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9

The Molecular Tumor Board Portal supports clinical decision..:

Tamborero, David ; Dienstmann, Rodrigo ; Rachid, Maan Haj...
Nature Cancer.  3 (2022)  2 - p. 251-261 , 2022
Link: https://doi.org/10.1038/..
 
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10

BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary ..:

Montalban, Gemma ; Bonache, Sandra ; Bach, Vanessa...
Cancer Genetics.  258-259 (2021)  - p. 10-17 , 2021
Link: https://doi.org/10.1016/..
 
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11

Patients' and professionals' perspective of non-in-person v..:

López-Fernández, Adrià ; Villacampa, Guillermo ; Grau, Elia...
Genetics in Medicine.  23 (2021)  8 - p. 1450-1457 , 2021
Link: https://doi.org/10.1038/..
 
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12

Genetic counsellors in a multidisciplinary model of clinica..:

López-Fernández, Adrià ; Serra-Juhé, Clara ; Balmaña, Judith.
Medicina Clínica (English Edition).  155 (2020)  2 - p. 77-81 , 2020
Link: https://doi.org/10.1016/..
 
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13

Risk of Cancer in Family Members of Patients with Lynch-Lik..:

Picó, María Dolores ; Sánchez-Heras, Ana Beatriz ; Castillejo, Adela...
Cancers.  12 (2020)  8 - p. 2225 , 2020
Link: https://doi.org/10.3390/..
 
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14

Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in..:

Sánchez-Heras, A. Beatriz ; Castillejo, Adela ; García-Díaz, Juan D....
Cancers.  12 (2020)  11 - p. 3277 , 2020
Link: https://doi.org/10.3390/..
 
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15

Computational Tools for Splicing Defect Prediction in Breas..:

Moles-Fernández, Alejandro ; Duran-Lozano, Laura ; Montalban, Gemma...
Frontiers in Genetics.  9 (2018)  - p. , 2018
Link: https://doi.org/10.3389/..
 
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