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Cancer Research, ISSN 0008-5472, 07/2016, Volume 76, Issue 14 Supplement, pp. 2563 - 2563
Background: Genome-wide association studies (GWAS) of bladder cancer risk recently identified several signals on chromosome 20p12.2 marked by single nucleotide... 
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2018, Volume 24, p. 29
Purpose: To determine genetic linkage between myopia and Han Chinese patients with a family history of the disease. Methods: One hundred seventy-six Han... 
Macular degeneration | Phenotypes | Myopia | Age
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2016, Volume 48, Issue 11, pp. 1330 - 1338
Journal Article
Cancer research, ISSN 0008-5472, 06/2019, Volume 79, Issue 11, pp. 2992 - 3000
Familial atypical multiple mole melanoma (FAMMM) syndrome is a hereditary cancer syndrome that results from mutations in several genes, including the gene. In... 
Journal Article
Journal Article
Journal Article
by Figueroa, J.D and Middlebrooks, C.D and Banday, A.R and Ye, Y and Garcia-Closas, M and Chatterjee, N and Koutros, S and Kiemeney, L.A and Rafnar, T and Bishop, T and Furberg, H and Matullo, G and Golka, K and Gago-Dominguez, M and Taylor, J.A and Fletcher, T and Siddiq, A and Cortessis, V.K and Kooperberg, C and Cussenot, O and Benhamou, S and Prescott, J and Porru, S and Dinney, C.P and Malats, N and Baris, D and Purdue, M.P and Jacobs, E.J and Albanes, D and Wang, Z and Chung, C.C and Vermeulen, S.H and Aben, K.K and Galesloot, T.E and Thorleifsson, G and Sulem, P and Stefansson, K and Kiltie, A.E and Harland, M and Teo, M and Offit, K and Vijai, J and Bajorin, D and Kopp, R and Fiorito, G and Guarrera, S and Sacerdote, C and Selinski, S and Hengstler, J.G and Gerullis, H and Ovsiannikov, D and Blaszkewicz, M and Castelao, J.E and Calaza, M and Martinez, M.E and Cordeiro, P and Xu, Z and Panduri, V and Kumar, R and Gurzau, E and Koppova, K and Bueno-de-Mesquita, H.B and Ljungberg, B and Clavel-Chapelon, F and Weiderpass, E and Krogh, V and Dorronsoro, M and Travis, R.C and Tjonneland, A and Brennan, P and Chang-Claude, J and Riboli, E and Conti, D and Stern, M.C and Pike, M.C and Berg, D and Yuan, J.M and Hohensee, C and Jeppson, R.P and Cancel-Tassin, G and Roupret, M and Comperat, E and Turman, C and Vivo, I. De and Giovannucci, E and Hunter, D.J and Kraft, P and Lindstrom, S and Carta, A and Pavanello, S and Arici, C and Mastrangelo, G and Kamat, A.M and Zhang, L and Gong, Y and Pu, X and Hutchinson, A and Burdett, L and Wheeler, W.A and Karagas, M.R and ... and Medicinska fakulteten and Urologi och andrologi and Institutionen för kirurgisk och perioperativ vetenskap and Umeå universitet
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 6, pp. 1203 - 1214
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2018, Volume 24, pp. 29 - 42
Purpose: To determine genetic linkage between myopia and Han Chinese patients with a family history of the disease. Methods: One hundred seventy-six Han... 
BREAST-CANCER | OCULAR REFRACTION | GENETIC POLYMORPHISMS | HTRA1 POLYMORPHISMS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUSCEPTIBILITY | OPHTHALMOLOGY | MACULAR DEGENERATION | RISK | SCAN | GENOME-WIDE ASSOCIATION | AGE
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 2, pp. 408 - 417
In oocytes with nondisjoined chromosomes 21 due to a meiosis I (MI) error, recombination is significantly reduced along chromosome 21; several lines of... 
MATERNAL AGE | ORIGIN | PRDM9 | MEIOTIC STAGE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | CROSSING-OVER | NONDISJUNCTION | RISK | POLYMORPHISM | CONFIGURATIONS | COMMON INVERSION | Meiosis - genetics | Oocytes - metabolism | Recombination, Genetic | Humans | Female | Chromosomes, Human, Pair 21 - genetics | Genome, Human | Nondisjunction, Genetic | Meiosis
Journal Article
01/2013, ISBN 9781303239175
Altered recombination count and placement along chromosome 21 have been identified as risk factors for nondisjunction (NDJ) which causes Trisomy 21. Hence, we... 
Biostatistics | Genetics | Epidemiology
Dissertation
Journal of Down Syndrome & chromosome abnormalities, ISSN 2472-1115, 12/2016, Volume 2, Issue 2
Variation in the zinc finger-binding domain (ZFBD) of the protein PR Domain-Containing Protein 9 (PRDM9) is associated with altered placement of recombination... 
Journal Article
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