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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 2
1995 1
1996 2
1997 1
1998 1
1999 1
2005 3
2006 2
2008 1
2009 6
2010 2
2011 5
2012 5
2013 7
2014 7
2015 4
2016 1
2017 1
2018 1
2019 1
2020 1
2021 4
2022 1
2023 1
2024 2

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56 results

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Page 1
Predisposition to aneuploidy in the oocyte.
Vialard F, Boitrelle F, Molina-Gomes D, Selva J. Vialard F, et al. Among authors: molina gomes d. Cytogenet Genome Res. 2011;133(2-4):127-35. doi: 10.1159/000324231. Epub 2011 Feb 17. Cytogenet Genome Res. 2011. PMID: 21335956 Review.
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Coignard J, Lush M, Beesley J, O'Mara TA, Dennis J, Tyrer JP, Barnes DR, McGuffog L, Leslie G, Bolla MK, Adank MA, Agata S, Ahearn T, Aittomäki K, Andrulis IL, Anton-Culver H, Arndt V, Arnold N, Aronson KJ, Arun BK, Augustinsson A, Azzollini J, Barrowdale D, Baynes C, Becher H, Bermisheva M, Bernstein L, Białkowska K, Blomqvist C, Bojesen SE, Bonanni B, Borg A, Brauch H, Brenner H, Burwinkel B, Buys SS, Caldés T, Caligo MA, Campa D, Carter BD, Castelao JE, Chang-Claude J, Chanock SJ, Chung WK, Claes KBM, Clarke CL; GEMO Study Collaborators; EMBRACE Collaborators; Collée JM, Conroy DM, Czene K, Daly MB, Devilee P, Diez O, Ding YC, Domchek SM, Dörk T, Dos-Santos-Silva I, Dunning AM, Dwek M, Eccles DM, Eliassen AH, Engel C, Eriksson M, Evans DG, Fasching PA, Flyger H, Fostira F, Friedman E, Fritschi L, Frost D, Gago-Dominguez M, Gapstur SM, Garber J, Garcia-Barberan V, García-Closas M, García-Sáenz JA, Gaudet MM, Gayther SA, Gehrig A, Georgoulias V, Giles GG, Godwin AK, Goldberg MS, Goldgar DE, González-Neira A, Greene MH, Guénel P, Haeberle L, Hahnen E, Haiman CA, Håkansson N, Hall P, Hamann U, Harrington PA, Hart SN, He W, Hogervorst FBL, Hollestelle A, Hopper JL, Horcasitas DJ, Hu… See abstract for full author list ➔ Coignard J, et al. Nat Commun. 2021 Feb 17;12(1):1078. doi: 10.1038/s41467-020-20496-3. Nat Commun. 2021. PMID: 33597508 Free PMC article.
Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
Ghieh F, Barbotin AL, Swierkowski-Blanchard N, Leroy C, Fortemps J, Gerault C, Hue C, Mambu Mambueni H, Jaillard S, Albert M, Bailly M, Izard V, Molina-Gomes D, Marcelli F, Prasivoravong J, Serazin V, Dieudonne MN, Delcroix M, Garchon HJ, Louboutin A, Mandon-Pepin B, Ferlicot S, Vialard F. Ghieh F, et al. Among authors: molina gomes d. Hum Reprod. 2022 May 30;37(6):1334-1350. doi: 10.1093/humrep/deac057. Hum Reprod. 2022. PMID: 35413094 Free PMC article.
Are leptin and adiponectin involved in recurrent pregnancy loss?
Serazin V, Duval F, Wainer R, Ravel C, Vialard F, Molina-Gomes D, Dieudonne MN, Dos Santos E. Serazin V, et al. Among authors: molina gomes d. J Obstet Gynaecol Res. 2018 Jun;44(6):1015-1022. doi: 10.1111/jog.13623. Epub 2018 Mar 14. J Obstet Gynaecol Res. 2018. PMID: 29536593
Williams-Beuren syndrome: the prenatal phenotype.
Popowski T, Vialard F, Leroy B, Bault JP, Molina-Gomes D. Popowski T, et al. Among authors: molina gomes d. Am J Obstet Gynecol. 2011 Dec;205(6):e6-8. doi: 10.1016/j.ajog.2011.09.017. Epub 2011 Sep 24. Am J Obstet Gynecol. 2011. PMID: 22000898
A genome-wide DNA methylation study in azoospermia.
Ferfouri F, Boitrelle F, Ghout I, Albert M, Molina Gomes D, Wainer R, Bailly M, Selva J, Vialard F. Ferfouri F, et al. Among authors: molina gomes d. Andrology. 2013 Nov;1(6):815-21. doi: 10.1111/j.2047-2927.2013.00117.x. Epub 2013 Aug 28. Andrology. 2013. PMID: 23996935 Free article.
Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene.
Quilichini J, Perol S, Cuisset L, Grotto S, Fouveaut C, Barbot JC, Verebi C, Jordan P, Héron D, Molina-Gomes D, Pipiras E, Grynberg M, Catteau-Jonard S, Touraine P, Christin-Maître S, Plu-Bureau G, El Khattabi L, Bienvenu T. Quilichini J, et al. Among authors: molina gomes d. Am J Med Genet A. 2024 Apr;194(4):e63479. doi: 10.1002/ajmg.a.63479. Epub 2023 Nov 21. Am J Med Genet A. 2024. PMID: 37987117
Are de novo rea(21;21) chromosomes really de novo?
Hervé B, Quibel T, Taieb S, Ruiz M, Molina-Gomes D, Vialard F. Hervé B, et al. Among authors: molina gomes d. Clin Case Rep. 2015 Oct;3(10):786-9. doi: 10.1002/ccr3.341. Epub 2015 Aug 26. Clin Case Rep. 2015. PMID: 26509006 Free PMC article.
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.
Figlioli G, Bogliolo M, Catucci I, Caleca L, Lasheras SV, Pujol R, Kiiski JI, Muranen TA, Barnes DR, Dennis J, Michailidou K, Bolla MK, Leslie G, Aalfs CM; ABCTB Investigators; Adank MA, Adlard J, Agata S, Cadoo K, Agnarsson BA, Ahearn T, Aittomäki K, Ambrosone CB, Andrews L, Anton-Culver H, Antonenkova NN, Arndt V, Arnold N, Aronson KJ, Arun BK, Asseryanis E, Auber B, Auvinen P, Azzollini J, Balmaña J, Barkardottir RB, Barrowdale D, Barwell J, Beane Freeman LE, Beauparlant CJ, Beckmann MW, Behrens S, Benitez J, Berger R, Bermisheva M, Blanco AM, Blomqvist C, Bogdanova NV, Bojesen A, Bojesen SE, Bonanni B, Borg A, Brady AF, Brauch H, Brenner H, Brüning T, Burwinkel B, Buys SS, Caldés T, Caliebe A, Caligo MA, Campa D, Campbell IG, Canzian F, Castelao JE, Chang-Claude J, Chanock SJ, Claes KBM, Clarke CL, Collavoli A, Conner TA, Cox DG, Cybulski C, Czene K, Daly MB, de la Hoya M, Devilee P, Diez O, Ding YC, Dite GS, Ditsch N, Domchek SM, Dorfling CM, Dos-Santos-Silva I, Durda K, Dwek M, Eccles DM, Ekici AB, Eliassen AH, Ellberg C, Eriksson M, Evans DG, Fasching PA, Figueroa J, Flyger H, Foulkes WD, Friebel TM, Friedman E, Gabrielson M, Gaddam P, Gago-Dominguez M, Gao C, Gapstur SM, G… See abstract for full author list ➔ Figlioli G, et al. NPJ Breast Cancer. 2019 Nov 1;5:38. doi: 10.1038/s41523-019-0127-5. eCollection 2019. NPJ Breast Cancer. 2019. PMID: 31700994 Free PMC article.
56 results