A citation-based method for searching scientific literature

Sami Belhadj, Pilar Mur, Matilde Navarro, Sara González, Victor Moreno, Gabriel Capellá, Laura Valle. Clin Gastroenterol Hepatol 2017
Times Cited: 29



Robbert D A Weren, Marjolijn J L Ligtenberg, C Marleen Kets, Richarda M de Voer, Eugène T P Verwiel, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Marjolijn C Jongmans, Christian Gilissen, Jayne Y Hehir-Kwa, Alexander Hoischen, Jay Shendure, Evan A Boyle, Eveline J Kamping, Iris D Nagtegaal, Bastiaan B J Tops, Fokko M Nagengast, Ad Geurts van Kessel, J Han J M van Krieken, Roland P Kuiper, Nicoline Hoogerbrugge. Nat Genet 2015
Times Cited: 229




List of shared articles



Times cited

Use of Family History and Genetic Testing to Determine Risk of Colorectal Cancer.
Fay Kastrinos, N Jewel Samadder, Randall W Burt. Gastroenterology 2020
24

Evaluation of Classic, Attenuated, and Oligopolyposis of the Colon.
Jessica M Long, Jacquelyn M Powers, Bryson W Katona. Gastrointest Endosc Clin N Am 2022
0

[MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer Institute (INCa)].
Marie-Pierre Buisine, Valérie Bonadona, Stéphanie Baert-Desurmont, Delphine Bonnet, Florence Coulet, Marion Dhooge, Jean-Christophe Saurin, Audrey Remenieras, Yves-Jean Bignon, Olivier Caron,[...]. Bull Cancer 2020
0

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
Judith E Grolleman, Richarda M de Voer, Fadwa A Elsayed, Maartje Nielsen, Robbert D A Weren, Claire Palles, Marjolijn J L Ligtenberg, Janet R Vos, Sanne W Ten Broeke, Noel F C C de Miranda,[...]. Cancer Cell 2019
80

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations.
Florentia Fostira, Emmanouil Kontopodis, Paraskevi Apostolou, Maria Fragkaki, Nikolaos Androulakis, Drakoulis Yannoukakos, Irene Konstantopoulou, Emmanouil Saloustros. Clin Genet 2018
18

Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
Pilar Mur, Ann-Sofie Jemth, Luka Bevc, Nuno Amaral, Matilde Navarro, Rafael Valdés-Mas, Tirso Pons, Gemma Aiza, Miguel Urioste, Alfonso Valencia,[...]. Hum Mutat 2018
6

How many is too many? Polyposis syndromes and what to do next.
Nina Gupta, Christine Drogan, Sonia S Kupfer. Curr Opin Gastroenterol 2022
0

Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
Flavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, Gwendoline Lienard, Stéphanie Vasseur, Sandrine Manase, Michel Bahuau, Emmanuelle Barouk Simonet, Virginie Bubien, Florence Coulet,[...]. Clin Genet 2021
3

Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1- and MSH3-associated polyposes.
Mariona Terradas, Pau M Munoz-Torres, Sami Belhadj, Gemma Aiza, Matilde Navarro, Joan Brunet, Gabriel Capellá, Laura Valle. Hum Mutat 2019
18

National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract.
Marion Dhooge, Stéphanie Baert-Desurmont, Carole Corsini, Olivier Caron, Nadine Andrieu, Pascaline Berthet, Valérie Bonadona, Odile Cohen-Haguenauer, Antoine De Pauw, Capucine Delnatte,[...]. Eur J Med Genet 2020
4

Six case reports of NTHL1-associated tumor syndrome further support it as a multi-tumor predisposition syndrome.
Chelsey B Weatherill, Sarah A Burke, Carolyn G Haskins, Darcy K Berry, Jeanne P Homer, Michael J Demeure, Sourat Darabi. Clin Genet 2022
0

Update on genetic predisposition to colorectal cancer and polyposis.
Laura Valle, Richarda M de Voer, Yael Goldberg, Wenche Sjursen, Asta Försti, Clara Ruiz-Ponte, Trinidad Caldés, Pilar Garré, Maren F Olsen, Margareta Nordling,[...]. Mol Aspects Med 2019
70

Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review.
S H Beck, A M Jelsig, H M Yassin, L J Lindberg, K A W Wadt, J G Karstensen. Fam Cancer 2022
1

Prevalence and Characterization of Biallelic and Monoallelic NTHL1 and MSH3 Variant Carriers From a Pan-Cancer Patient Population.
Erin E Salo-Mullen, Anna Maio, Semanti Mukherjee, Chaitanya Bandlamudi, Jinru Shia, Yelena Kemel, Karen A Cadoo, Ying Liu, Maria Carlo, Megha Ranganathan,[...]. JCO Precis Oncol 2021
5

Co-occurrence of breast cancer and neuroendocrine tumours: New genetic insights beyond Multiple Endocrine Neoplasia syndromes.
Vincent Larouche, Amit Akirov, Emily Thain, Raymond H Kim, Shereen Ezzat. Endocrinol Diabetes Metab 2019
7


NTHL1-associate polyposis: first Australian case report.
Alexandra Groves, Margaret Gleeson, Allan D Spigelman. Fam Cancer 2019
14

MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer institute (INCa).
Chrystelle Colas, Valérie Bonadona, Stéphanie Baert-Desurmont, Delphine Bonnet, Florence Coulet, Marion Dhooge, Jean-Christophe Saurin, Audrey Remenieras, Yves-Jean Bignon, Olivier Caron,[...]. Eur J Med Genet 2020
8

NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Sami Belhadj, Isabel Quintana, Pilar Mur, Pau M Munoz-Torres, M Henar Alonso, Matilde Navarro, Mariona Terradas, Virginia Piñol, Joan Brunet, Victor Moreno,[...]. Sci Rep 2019
16

Development, technical validation, and clinical application of a multigene panel for hereditary gastrointestinal cancer and polyposis.
Maria Teresa Ricci, Sara Volorio, Stefano Signoroni, Paolo Mariani, Frederique Mariette, Domenico Sardella, Valeria Pensotti, Marco Vitellaro. Tumori 2019
3

The Inherited and Familial Component of Early-Onset Colorectal Cancer.
Maria Daca Alvarez, Isabel Quintana, Mariona Terradas, Pilar Mur, Francesc Balaguer, Laura Valle. Cells 2021
16

Caught in motion: human NTHL1 undergoes interdomain rearrangement necessary for catalysis.
Brittany L Carroll, Karl E Zahn, John P Hanley, Susan S Wallace, Julie A Dragon, Sylvie Doublié. Nucleic Acids Res 2021
3

Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.
Víctor Lorca, Daniel Rueda, Lorena Martín-Morales, María Jesús Fernández-Aceñero, Judith Grolleman, Carmen Poves, Patricia Llovet, Sandra Tapial, Vanesa García-Barberán, Julián Sanz,[...]. Sci Rep 2019
5

NTHL1 and MUTYH polyposis syndromes: two sides of the same coin?
Robbert DA Weren, Marjolijn Jl Ligtenberg, Ad Geurts van Kessel, Richarda M De Voer, Nicoline Hoogerbrugge, Roland P Kuiper. J Pathol 2018
41

Current status of the genetic susceptibility in attenuated adenomatous polyposis.
Víctor Lorca, Pilar Garre. World J Gastrointest Oncol 2019
2