المؤلفون: Benyamin, Beben, Maihofer, Adam X, Schork, Andrew J, Hamilton, Bruce A, Rao, Fangwen, Schmid-Schönbein, Geert W, Zhang, Kuixing, Mahata, Manjula, Stridsberg, Mats, Schork, Nicholas J, Biswas, Nilima, Hook, Vivian Y, Wei, Zhiyun, Montgomery, Grant W, Martin, Nicholas G, Nievergelt, Caroline M, Whitfield, John B, O’Connor, Daniel T

المصدر: Human Molecular Genetics. 26(1)

مصطلحات موضوعية: Adolescent, Adrenal Glands, Adult, Aged, Animals, Australia, Biomarkers, Catecholamines, Cells, Cultured, Chromaffin Cells, Chromogranin A, Factor XII, Female, Genetic Loci, Genome-Wide Association Study, Humans, Hypertension, Kallikreins, Male, Mice, Middle Aged, Peptide Fragments, Rats, United States, Young Adult, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4qq2h46wTest

المؤلفون: Painter, Jodie N, O'Mara, Tracy A, Batra, Jyotsna, Cheng, Timothy, Lose, Felicity A, Dennis, Joe, Michailidou, Kyriaki, Tyrer, Jonathan P, Ahmed, Shahana, Ferguson, Kaltin, Healey, Catherine S, Kaufmann, Susanne, Hillman, Kristine M, Walpole, Carina, Moya, Leire, Pollock, Pamela, Jones, Angela, Howarth, Kimberley, Martin, Lynn, Gorman, Maggie, Hodgson, Shirley, De Polanco, Ma Magdalena Echeverry, Sans, Monica, Carracedo, Angel, Castellvi-Bel, Sergi, Rojas-Martinez, Augusto, Santos, Erika, Teixeira, Manuel R, Carvajal-Carmona, Luis, Shu, Xiao-Ou, Long, Jirong, Zheng, Wei, Xiang, Yong-Bing, Montgomery, Grant W, Webb, Penelope M, Scott, Rodney J, McEvoy, Mark, Attia, John, Holliday, Elizabeth, Martin, Nicholas G, Nyholt, Dale R, Henders, Anjali K, Fasching, Peter A, Hein, Alexander, Beckmann, Matthias W, Renner, Stefan P, Dörk, Thilo, Hillemanns, Peter, Dürst, Matthias, Runnebaum, Ingo, Lambrechts, Diether, Coenegrachts, Lieve, Schrauwen, Stefanie, Amant, Frederic, Winterhoff, Boris, Dowdy, Sean C, Goode, Ellen L, Teoman, Attila, Salvesen, Helga B, Trovik, Jone, Njolstad, Tormund S, Werner, Henrica MJ, Ashton, Katie, Proietto, Tony, Otton, Geoffrey, Tzortzatos, Gerasimos, Mints, Miriam, Tham, Emma, Hall, Per, Czene, Kamila, Liu, Jianjun, Li, Jingmei, Hopper, John L, Southey, Melissa C, Ekici, Arif B, Ruebner, Matthias, Johnson, Nicola, Peto, Julian, Burwinkel, Barbara, Marme, Frederik, Brenner, Hermann, Dieffenbach, Aida K, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Depreeuw, Jeroen, Moisse, Matthieu, Chang-Claude, Jenny, Rudolph, Anja, Couch, Fergus J, Olson, Janet E, Giles, Graham G, Bruinsma, Fiona, Cunningham, Julie M, Fridley, Brooke L, Børresen-Dale, Anne-Lise, Kristensen, Vessela N, Cox, Angela, Swerdlow, Anthony J, Orr, Nicholas

المصدر: Human Molecular Genetics. 24(5)

مصطلحات موضوعية: Cancer, Biotechnology, Human Genome, Prevention, Genetics, 2.1 Biological and endogenous factors, Aetiology, Alleles, Case-Control Studies, Cell Line, Tumor, Chromosome Mapping, Computational Biology, Databases, Genetic, Endometrial Neoplasms, Epigenesis, Genetic, Female, Genetic Loci, Genetic Variation, Genome-Wide Association Study, Genotype, Haplotypes, Hepatocyte Nuclear Factor 1-beta, Humans, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Promoter Regions, Genetic, RNA, Messenger, Risk Factors, White People, National Study of Endometrial Cancer Genetics Group, CHIBCHA Consortium, Australian National Endometrial Cancer Study Group, RENDOCAS, Australian Ovarian Cancer Study, GENICA Network, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8dj6n115Test

المؤلفون: David A. Hume, Nicholas G. Martin, V. K. Chundru, Allan F. McRae, Naomi R. Wray, A. J. Beveridge, Grant W. Montgomery, Riccardo E. Marioni, Ian J. Deary, Peter M. Visscher, J. G. D. Prendergast, Tian Lin

المصدر: Chundru, V K, Marioni, R E, Prendergast, J, Lin, T, Beveridge, A J, Martin, N G, Montgomery, G W, Hume, D A, Deary, I J, Visscher, P M, Wray, N R & McRae, A F 2023, ' Rare genetic variants underlie outlying levels of DNA methylation and gene-expression ', Human Molecular Genetics, vol. 32, no. 11, pp. 1912-1921 . https://doi.org/10.1093/hmg/ddad028Test

مصطلحات موضوعية: Genetics, education.field_of_study, Population, Genetic variants, dNaM, General Medicine, Biology, Phenotype, Genome, Genetic variation, Gene expression, DNA methylation, education, Molecular Biology, Genetics (clinical)

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3271219cb84b72a63728ee09a14d6a6fTest
https://doi.org/10.1093/hmg/ddad028Test

المؤلفون: Siddiq, Afshan, Couch, Fergus J, Chen, Gary K, Lindström, Sara, Eccles, Diana, Millikan, Robert C, Michailidou, Kyriaki, Stram, Daniel O, Beckmann, Lars, Rhie, Suhn Kyong, Ambrosone, Christine B, Aittomäki, Kristiina, Amiano, Pilar, Apicella, Carmel, Investigators, Australian Breast Cancer Tissue Bank, Baglietto, Laura, Bandera, Elisa V, Beckmann, Matthias W, Berg, Christine D, Bernstein, Leslie, Blomqvist, Carl, Brauch, Hiltrud, Brinton, Louise, Bui, Quang M, Buring, Julie E, Buys, Saundra S, Campa, Daniele, Carpenter, Jane E, Chasman, Daniel I, Chang-Claude, Jenny, Chen, Constance, Clavel-Chapelon, Françoise, Cox, Angela, Cross, Simon S, Czene, Kamila, Deming, Sandra L, Diasio, Robert B, Diver, W Ryan, Dunning, Alison M, Durcan, Lorraine, Ekici, Arif B, Fasching, Peter A, Study, Familial Breast Cancer, Feigelson, Heather Spencer, Fejerman, Laura, Figueroa, Jonine D, Fletcher, Olivia, Flesch-Janys, Dieter, Gaudet, Mia M, Consortium, The GENICA, Gerty, Susan M, Rodriguez-Gil, Jorge L, Giles, Graham G, van Gils, Carla H, Godwin, Andrew K, Graham, Nikki, Greco, Dario, Hall, Per, Hankinson, Susan E, Hartmann, Arndt, Hein, Rebecca, Heinz, Judith, Hoover, Robert N, Hopper, John L, Hu, Jennifer J, Huntsman, Scott, Ingles, Sue A, Irwanto, Astrid, Isaacs, Claudine, Jacobs, Kevin B, John, Esther M, Justenhoven, Christina, Kaaks, Rudolf, Kolonel, Laurence N, Coetzee, Gerhard A, Lathrop, Mark, Le Marchand, Loic, Lee, Adam M, Lee, I-Min, Lesnick, Timothy, Lichtner, Peter, Liu, Jianjun, Lund, Eiliv, Makalic, Enes, Martin, Nicholas G, McLean, Catriona A, Meijers-Heijboer, Hanne, Meindl, Alfons, Miron, Penelope, Monroe, Kristine R, Montgomery, Grant W, Müller-Myhsok, Bertram, Nickels, Stefan, Nyante, Sarah J, Olswold, Curtis, Overvad, Kim, Palli, Domenico, Park, Daniel J, Palmer, Julie R, Pathak, Harsh

المصدر: Human Molecular Genetics. 21(24)

مصطلحات موضوعية: Biological Sciences, Genetics, Clinical Research, Aging, Human Genome, Breast Cancer, Cancer, Aetiology, 2.1 Biological and endogenous factors, Breast Neoplasms, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Receptors, Estrogen, Australian Breast Cancer Tissue Bank Investigators, Familial Breast Cancer Study, GENICA Consortium, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5q1884jrTest

المؤلفون: Spain, Sarah L, Carvajal-Carmona, Luis G, Howarth, Kimberley M, Jones, Angela M, Su, Zhan, Cazier, Jean-Baptiste, Williams, Jennet, Aaltonen, Lauri A, Pharoah, Paul, Kerr, David J, Cheadle, Jeremy, Li, Li, Casey, Graham, Vodicka, Pavel, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G, Montgomery, Grant W, Young, Joanne, Baird, Paul N, Morreau, Hans, van Wezel, Tom, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, Dunlop, Malcolm, Houlston, Richard S, Tomlinson, Ian PM

المصدر: Human Molecular Genetics. 21(4)

مصطلحات موضوعية: Genetics, Colo-Rectal Cancer, Aging, Digestive Diseases, Human Genome, Biotechnology, Cancer, Aetiology, 2.1 Biological and endogenous factors, Chromosome Mapping, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 12, Colorectal Neoplasms, Computational Biology, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotyping Techniques, Haplotypes, Humans, Logistic Models, Polymorphism, Single Nucleotide, Software, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3vp23900Test

المؤلفون: Macgregor, Stuart, Hewitt, Alex W, Hysi, Pirro G, Ruddle, Jonathan B, Medland, Sarah E, Henders, Anjali K, Gordon, Scott D, Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G, Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L, Craig, Jamie E, Montgomery, Grant W, Tran-Viet, Khanh-Nhat, Brown, Nadean L, Spector, Timothy D, Martin, Nicholas G, Young, Terri L, Hammond, Christopher J, Mackey, David A

المصدر: Human Molecular Genetics. 19(13)

مصطلحات موضوعية: Eye Disease and Disorders of Vision, Neurosciences, Human Genome, Clinical Research, Genetics, 2.1 Biological and endogenous factors, Aetiology, Eye, Adolescent, Adult, Aged, Aged, 80 and over, Australia, Basic Helix-Loop-Helix Transcription Factors, Blindness, Child, Child, Preschool, Genome-Wide Association Study, Humans, Membrane Proteins, Middle Aged, Optic Disk, Optic Nerve, Polymorphism, Single Nucleotide, Twins, United Kingdom, Young Adult, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/294404qjTest

المؤلفون: Chundru, V Kartik, Marioni, Riccardo E, Prendergast, James G D, Lin, Tian, Beveridge, Allan J, Martin, Nicholas G, Montgomery, Grant W, Hume, David A, Deary, Ian J, Visscher, Peter M, Wray, Naomi R, McRae, Allan F

المصدر: Human Molecular Genetics; Jun2023, Vol. 32 Issue 11, p1912-1921, 10p

المؤلفون: Asma M Aman, Luis M García-Marín, Jackson G Thorp, Adrian I Campos, Gabriel Cuellar-Partida, Nicholas G Martin, Miguel E Rentería

المصدر: Human molecular genetics. 31(17)

مصطلحات موضوعية: Depression, Genetics, Humans, Genetic Predisposition to Disease, General Medicine, Obesity, Phenomics, Molecular Biology, Polymorphism, Single Nucleotide, Genetics (clinical), Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e17d5c254b3c45d205942bb7f23b754Test
https://pubmed.ncbi.nlm.nih.gov/35394011Test

المؤلفون: Nicholas K. Hayward, Robyn P. M. Saw, Jonathan R. Stretch, Kerwin F. Shannon, Grant W. Montgomery, Matthew Law, Antonia L. Pritchard, Jane M. Palmer, Kiarash Khosrotehrani, David L. Duffy, Graham J. Mann, Anne E. Cust, Peter Johansson, Nicholas G. Martin, Richard A. Scolyer, John F. Thompson, Georgina V. Long, Lauren G. Aoude, Andrew J. Spillane, Mark M. Iles, Stuart MacGregor

المصدر: Human Molecular Genetics

مصطلحات موضوعية: AcademicSubjects/SCI01140, Male, Multifactorial Inheritance, Skin Neoplasms, Ultraviolet Rays, Penetrance, Biology, medicine.disease_cause, Germline, 03 medical and health sciences, 0302 clinical medicine, CDKN2A, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Association Studies Article, Molecular Biology, neoplasms, Melanoma, Genetics (clinical), Alleles, Cyclin-Dependent Kinase Inhibitor p16, Germ-Line Mutation, 030304 developmental biology, Whole genome sequencing, 0303 health sciences, Mutation, General Medicine, medicine.disease, 030220 oncology & carcinogenesis, Cutaneous melanoma, Etiology, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c26eb2702a938ee4d5606f15869cab6Test
http://europepmc.org/articles/PMC7566496Test

المؤلفون: Aman, Asma M, García-Marín, Luis M, Thorp, Jackson G, Campos, Adrian I, Cuellar-Partida, Gabriel, Martin, Nicholas G, Rentería, Miguel E

المصدر: Human Molecular Genetics; 9/1/2022, Vol. 31 Issue 17, p2887-2898, 12p