121 related articles for article (PubMed ID: 37456212)
1. A Novel Germline Pathogenic Variant of
Amin M; Mahmoodi-Khaledi E; Narrei S; Zeinalian M
Iran J Med Sci; 2023 Jul; 48(4):420-424. PubMed ID: 37456212
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing identifies RASSF1 and KLK3 germline variants in an Iranian multiple-case breast cancer family.
Radmanesh H; Liu D; Geffers R; Shandiz FH; Sadr-Nabavi A; Hillemanns P; Park-Simon TW; Dörk T
Eur J Med Genet; 2022 Mar; 65(3):104425. PubMed ID: 35032689
[TBL] [Abstract][Full Text] [Related]
3. Novel candidate genes may be possible predisposing factors revealed by whole exome sequencing in familial esophageal squamous cell carcinoma.
Forouzanfar N; Baranova A; Milanizadeh S; Heravi-Moussavi A; Jebelli A; Abbaszadegan MR
Tumour Biol; 2017 May; 39(5):1010428317699115. PubMed ID: 28459198
[TBL] [Abstract][Full Text] [Related]
4. Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes.
Golyan FF; Druley TE; Abbaszadegan MR
Clin Transl Oncol; 2020 May; 22(5):681-693. PubMed ID: 31321674
[TBL] [Abstract][Full Text] [Related]
5. Germline likely pathogenic variants in ataxia-telangiectasia-mutated gene in an Iranian family with hereditary diffuse gastric cancer without
Kheirollahi M; Saneipour M; Moridnia A
J Cancer Res Ther; 2021; 17(6):1434-1437. PubMed ID: 34916374
[TBL] [Abstract][Full Text] [Related]
6. Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia.
Ansari H; Mohammadi-Asl J; Hajjari M; Tahmasebi-Birgani M; Kollaee A; Jassemi-Zergani F; Vakili-Hajiagha A
J Gene Med; 2019 Aug; 21(8):e3103. PubMed ID: 31177591
[TBL] [Abstract][Full Text] [Related]
7. Enrichment of heterozygous germline
Maciaszek JL; Oak N; Chen W; Hamilton KV; McGee RB; Nuccio R; Mostafavi R; Hines-Dowell S; Harrison L; Taylor L; Gerhardt EL; Ouma A; Edmonson MN; Patel A; Nakitandwe J; Pappo AS; Azzato EM; Shurtleff SA; Ellison DW; Downing JR; Hudson MM; Robison LL; Santana V; Newman S; Zhang J; Wang Z; Wu G; Nichols KE; Kesserwan CA
Cold Spring Harb Mol Case Stud; 2019 Oct; 5(5):. PubMed ID: 31604778
[TBL] [Abstract][Full Text] [Related]
8. Clinical implications of germline mutations in breast cancer genes: RECQL.
Bowden AR; Tischkowitz M
Breast Cancer Res Treat; 2019 Apr; 174(3):553-560. PubMed ID: 30610487
[TBL] [Abstract][Full Text] [Related]
9. De novo myelodysplastic syndrome in a Rothmund-Thomson Syndrome patient with novel pathogenic
Jiang C; Zhang H; Zhao C; Wang L; Hu X; Pan Z
Blood Sci; 2023 Apr; 5(2):125-130. PubMed ID: 37228773
[TBL] [Abstract][Full Text] [Related]
10. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
[TBL] [Abstract][Full Text] [Related]
11. Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families.
Shahi RB; De Brakeleer S; Caljon B; Pauwels I; Bonduelle M; Joris S; Fontaine C; Vanhoeij M; Van Dooren S; Teugels E; De Grève J
BMC Cancer; 2019 Apr; 19(1):313. PubMed ID: 30947698
[TBL] [Abstract][Full Text] [Related]
12. Whole-exome analysis of a Li-Fraumeni family trio with a novel TP53 PRD mutation and anticipation profile.
Franceschi S; Spugnesi L; Aretini P; Lessi F; Scarpitta R; Galli A; Congregati C; Caligo MA; Mazzanti CM
Carcinogenesis; 2017 Sep; 38(9):938-943. PubMed ID: 28911001
[TBL] [Abstract][Full Text] [Related]
13. Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
Zhang JX; Fu L; de Voer RM; Hahn MM; Jin P; Lv CX; Verwiel ET; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; Sheng JQ; Geurts van Kessel A
World J Gastroenterol; 2015 Apr; 21(14):4136-49. PubMed ID: 25892863
[TBL] [Abstract][Full Text] [Related]
14. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.
Sarmadi A; Nasrniya S; Narrei S; Nouri Z; Abtahi H; Tabatabaiefar MA
Mol Biol Rep; 2020 Jul; 47(7):5355-5364. PubMed ID: 32623615
[TBL] [Abstract][Full Text] [Related]
15. Omic Approach in Non-smoker Female with Lung Squamous Cell Carcinoma Pinpoints to Germline Susceptibility and Personalized Medicine.
Baldassarri M; Fallerini C; Cetta F; Ghisalberti M; Bellan C; Furini S; Spiga O; Crispino S; Gotti G; Ariani F; Paladini P; Renieri A; Frullanti E
Cancer Res Treat; 2018 Apr; 50(2):356-365. PubMed ID: 28546520
[TBL] [Abstract][Full Text] [Related]
16. Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation.
Malakootian M; Jalilian M; Kalayinia S; Hosseini Moghadam M; Heidarali M; Haghjoo M
BMC Cardiovasc Disord; 2022 Feb; 22(1):37. PubMed ID: 35148685
[TBL] [Abstract][Full Text] [Related]
17. A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing.
Ghasemi S; Mahdavi M; Maleki M; Salahshourifar I; Kalayinia S
BMC Med Genomics; 2022 Nov; 15(1):234. PubMed ID: 36344977
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel pathogenic variant in
Fazelifar AF; Pourirahim M; Masoumi T; Biglari A; Maleki M; Kalayinia S
J Arrhythm; 2023 Jun; 39(3):430-453. PubMed ID: 37324772
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of RECQL4 gene variant in a child with Rothmund-Thomson syndrome].
Wu Q; Weng W; Yuan J; Xu X; Huang K; Dong G; Fu J; Wu W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):31-34. PubMed ID: 34964962
[TBL] [Abstract][Full Text] [Related]
20. RECQL5: Another DNA helicase potentially involved in hereditary breast cancer susceptibility.
Tavera-Tapia A; de la Hoya M; Calvete O; Martin-Gimeno P; Fernández V; Macías JA; Alonso B; Pombo L; de Diego C; Alonso R; Pita G; Barroso A; Urioste M; Caldés T; Newman JA; Benítez J; Osorio A
Hum Mutat; 2019 May; 40(5):566-577. PubMed ID: 30817846
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
