186 related articles for article (PubMed ID: 37507557)
41. Incidence of Germline Variants in Familial Bladder Cancer and Among Patients With Cancer Predisposition Syndromes.
Mossanen M; Nassar AH; Stokes SM; Martinez-Chanza N; Kumar V; Nuzzo PV; Kwiatkowski DJ; Garber JE; Curran C; Freeman D; Preston M; Mouw KW; Kibel A; Choueiri TK; Sonpavde G; Rana HQ
Clin Genitourin Cancer; 2022 Dec; 20(6):568-574. PubMed ID: 36127252
[TBL] [Abstract][Full Text] [Related]
42. Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer.
Wagener R; Taeubner J; Walter C; Yasin L; Alzoubi D; Bartenhagen C; Attarbaschi A; Classen CF; Kontny U; Hauer J; Fischer U; Dugas M; Kuhlen M; Borkhardt A; Brozou T
Eur J Hum Genet; 2021 Aug; 29(8):1301-1311. PubMed ID: 33840814
[TBL] [Abstract][Full Text] [Related]
43. Cancer predisposition and germline CTNNA1 variants.
Lobo S; Benusiglio PR; Coulet F; Boussemart L; Golmard L; Spier I; Hüneburg R; Aretz S; Colas C; Oliveira C
Eur J Med Genet; 2021 Oct; 64(10):104316. PubMed ID: 34425242
[TBL] [Abstract][Full Text] [Related]
44. Germline pathogenic variants in 786 neuroblastoma patients.
Kim J; Vaksman Z; Egolf LE; Kaufman R; Evans JP; Conkrite KL; Danesh A; Lopez G; Randall MP; Dent MH; Farra LM; Menghani N; Dymek M; Desai H; Hausler R; ; ; ; Auvil JG; Gerhard DS; Hakonarson H; Maxwell KN; Cole KA; Pugh TJ; Bosse KR; Khan J; Wei JS; Maris JM; Stewart DR; Diskin SJ
medRxiv; 2023 Jan; ():. PubMed ID: 36747619
[TBL] [Abstract][Full Text] [Related]
45. Cancer Susceptibility Mutations in Patients With Urothelial Malignancies.
Carlo MI; Ravichandran V; Srinavasan P; Bandlamudi C; Kemel Y; Ceyhan-Birsoy O; Mukherjee S; Mandelker D; Chaim J; Knezevic A; Rana S; Fnu Z; Breen K; Arnold AG; Khurram A; Tkachuk K; Cipolla CK; Regazzi A; Hakimi AA; Al-Ahmadie H; Dalbagni G; Cadoo KA; Walsh MF; Teo MY; Funt SA; Coleman JA; Bochner BH; Iyer G; Solit DB; Stadler ZK; Zhang L; Rosenberg JE; Taylor BS; Robson ME; Berger MF; Vijai J; Bajorin DF; Offit K
J Clin Oncol; 2020 Feb; 38(5):406-414. PubMed ID: 31794323
[TBL] [Abstract][Full Text] [Related]
46. DICER1 Syndrome: Characterization of the Ocular Phenotype in a Family-Based Cohort Study.
Huryn LA; Turriff A; Harney LA; Carr AG; Chevez-Barrios P; Gombos DS; Ram R; Hufnagel RB; Hill DA; Zein WM; Schultz KAP; Bishop R; Stewart DR
Ophthalmology; 2019 Feb; 126(2):296-304. PubMed ID: 30339877
[TBL] [Abstract][Full Text] [Related]
47. Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition.
Gambale A; Russo R; Andolfo I; Quaglietta L; De Rosa G; Contestabile V; De Martino L; Genesio R; Pignataro P; Giglio S; Capasso M; Parasole R; Pasini B; Iolascon A
Clin Genet; 2019 Oct; 96(4):359-365. PubMed ID: 31278746
[TBL] [Abstract][Full Text] [Related]
48. Identification of germline cancer predisposition variants in pediatric sarcoma patients from somatic tumor testing.
Alba-Pavón P; Alaña L; Gutierrez-Jimeno M; García-Obregón S; Imízcoz T; Panizo E; González-Urdiales P; Echebarria-Barona A; Lopez Almaraz R; Zaldumbide L; Astigarraga I; Patiño-García A; Villate O
Sci Rep; 2023 Feb; 13(1):2959. PubMed ID: 36805510
[TBL] [Abstract][Full Text] [Related]
49. Evaluation of the pathogenic potential of germline DDX41 variants in hematopoietic neoplasms using the ACMG/AMP guidelines.
Matsui H; Hirata M
Int J Hematol; 2024 May; 119(5):552-563. PubMed ID: 38492200
[TBL] [Abstract][Full Text] [Related]
50. High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome.
de Kock L; Wang YC; Revil T; Badescu D; Rivera B; Sabbaghian N; Wu M; Weber E; Sandoval C; Hopman SM; Merks JH; van Hagen JM; Bouts AH; Plager DA; Ramasubramanian A; Forsmark L; Doyle KL; Toler T; Callahan J; Engelenberg C; Bouron-Dal Soglio D; Priest JR; Ragoussis J; Foulkes WD
J Med Genet; 2016 Jan; 53(1):43-52. PubMed ID: 26475046
[TBL] [Abstract][Full Text] [Related]
51. The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
Slavin TP; Neuhausen SL; Nehoray B; Niell-Swiller M; Solomon I; Rybak C; Blazer K; Adamson A; Yang K; Sand S; Guerrero-Llamas N; Castillo D; Herzog J; Wu X; Tao S; Raja S; Chung V; Singh G; Nadesan S; Brown S; Cruz-Correa M; Petersen GM; Weitzel J;
Fam Cancer; 2018 Apr; 17(2):235-245. PubMed ID: 28687971
[TBL] [Abstract][Full Text] [Related]
52. Multiple DICER1-related tumors in a child with a large interstitial 14q32 deletion.
de Kock L; Geoffrion D; Rivera B; Wagener R; Sabbaghian N; Bens S; Ellezam B; Bouron-Dal Soglio D; Ordóñez J; Sacharow S; Polo Nieto JF; Guillerman RP; Vujanic GM; Priest JR; Siebert R; Foulkes WD
Genes Chromosomes Cancer; 2018 May; 57(5):223-230. PubMed ID: 29315962
[TBL] [Abstract][Full Text] [Related]
53. Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma.
Abdel-Rahman MH; Sample KM; Pilarski R; Walsh T; Grosel T; Kinnamon D; Boru G; Massengill JB; Schoenfield L; Kelly B; Gordon D; Johansson P; DeBenedictis MJ; Singh A; Casadei S; Davidorf FH; White P; Stacey AW; Scarth J; Fewings E; Tischkowitz M; King MC; Hayward NK; Cebulla CM
Ophthalmology; 2020 May; 127(5):668-678. PubMed ID: 32081490
[TBL] [Abstract][Full Text] [Related]
54. Primary intracranial spindle cell sarcoma with rhabdomyosarcoma-like features share a highly distinct methylation profile and DICER1 mutations.
Koelsche C; Mynarek M; Schrimpf D; Bertero L; Serrano J; Sahm F; Reuss DE; Hou Y; Baumhoer D; Vokuhl C; Flucke U; Petersen I; Brück W; Rutkowski S; Zambrano SC; Garcia Leon JL; Diaz Coronado RY; Gessler M; Tirado OM; Mora J; Alonso J; Garcia Del Muro X; Esteller M; Sturm D; Ecker J; Milde T; Pfister SM; Korshunov A; Snuderl M; Mechtersheimer G; Schüller U; Jones DTW; von Deimling A
Acta Neuropathol; 2018 Aug; 136(2):327-337. PubMed ID: 29881993
[TBL] [Abstract][Full Text] [Related]
55. Germ line predisposition variants occur in myelodysplastic syndrome patients of all ages.
Feurstein S; Trottier AM; Estrada-Merly N; Pozsgai M; McNeely K; Drazer MW; Ruhle B; Sadera K; Koppayi AL; Scott BL; Oran B; Nishihori T; Agrawal V; Saad A; Lindsley RC; Nakamura R; Kim S; Hu Z; Sobecks R; Spellman S; Saber W; Godley LA
Blood; 2022 Dec; 140(24):2533-2548. PubMed ID: 35969835
[TBL] [Abstract][Full Text] [Related]
56. Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort Study.
Khan NE; Bauer AJ; Schultz KAP; Doros L; Decastro RM; Ling A; Lodish MB; Harney LA; Kase RG; Carr AG; Rossi CT; Field A; Harris AK; Williams GM; Dehner LP; Messinger YH; Hill DA; Stewart DR
J Clin Endocrinol Metab; 2017 May; 102(5):1614-1622. PubMed ID: 28323992
[TBL] [Abstract][Full Text] [Related]
57. Dental abnormalities in individuals with pathogenic germline variation in DICER1.
Choi S; Lee JS; Bassim CW; Kushner H; Carr AG; Gardner PJ; Harney LA; Schultz KAP; Stewart DR
Am J Med Genet A; 2019 Sep; 179(9):1820-1825. PubMed ID: 31313479
[TBL] [Abstract][Full Text] [Related]
58. Germline mutations in pediatric cancer cohort with mixed-ancestry Mexicans.
Alonso-Luna O; Mercado-Celis GE; Melendez-Zajgla J; Barquera R; Zapata-Tarres M; Juárez-Villegas LE; Mendoza-Caamal EC; Rey-Helo E; Borges-Yañez SA
Mol Genet Genomic Med; 2024 Jan; 12(1):e2332. PubMed ID: 38093606
[TBL] [Abstract][Full Text] [Related]
59. Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Garcia-Pelaez J; Barbosa-Matos R; Lobo S; Dias A; Garrido L; Castedo S; Sousa S; Pinheiro H; Sousa L; Monteiro R; Maqueda JJ; Fernandes S; Carneiro F; Pinto N; Lemos C; Pinto C; Teixeira MR; Aretz S; Bajalica-Lagercrantz S; Balmaña J; Blatnik A; Benusiglio PR; Blanluet M; Bours V; Brems H; Brunet J; Calistri D; Capellá G; Carrera S; Colas C; Dahan K; de Putter R; Desseignés C; Domínguez-Garrido E; Egas C; Evans DG; Feret D; Fewings E; Fitzgerald RC; Coulet F; Garcia-Barcina M; Genuardi M; Golmard L; Hackmann K; Hanson H; Holinski-Feder E; Hüneburg R; Krajc M; Lagerstedt-Robinson K; Lázaro C; Ligtenberg MJL; Martínez-Bouzas C; Merino S; Michils G; Novaković S; Patiño-García A; Ranzani GN; Schröck E; Silva I; Silveira C; Soto JL; Spier I; Steinke-Lange V; Tedaldi G; Tejada MI; Woodward ER; Tischkowitz M; Hoogerbrugge N; Oliveira C
Lancet Oncol; 2023 Jan; 24(1):91-106. PubMed ID: 36436516
[TBL] [Abstract][Full Text] [Related]
60. Cancer genetics-one family at a time.
Foulkes W
Clin Invest Med; 2019 Dec; 42(4):E7-E13. PubMed ID: 31922703
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
