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A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array
Schurz, Haiko, Kinnear, Craig J., Gignoux, Chris, Wojcik, Genevieve, van Helden, Paul D., Tromp, Gerard, Henn, Brenna, Hoal, Eileen G., Möller, Marlo
Published in Frontiers in genetics (18.01.2019)
Published in Frontiers in genetics (18.01.2019)
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Characterization of the Gray Whale Eschrichtius robustus Genome and a Genotyping Array Based on Single-Nucleotide Polymorphisms in Candidate Genes
DeWoody, J Andrew, Fernandez, Nadia B, Brüniche-Olsen, Anna, Antonides, Jennifer D, Doyle, Jacqueline M, San Miguel, Phillip, Westerman, Rick, Vertyankin, Vladimir V, Godard-Codding, Céline A J, Bickham, John W
Published in The Biological bulletin (Lancaster) (01.06.2017)
Published in The Biological bulletin (Lancaster) (01.06.2017)
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A Search for Variants Associated With Young-Onset Type 2 Diabetes in American Indians in a 100K Genotyping Array
Hanson, Robert L., Bogardus, Clifton, Duggan, David, Kobes, Sayuko, Knowlton, Michele, Infante, Aniello M., Marovich, Leslie, Benitez, Deb, Baier, Leslie J., Knowler, William C.
Published in Diabetes (New York, N.Y.) (01.12.2007)
Published in Diabetes (New York, N.Y.) (01.12.2007)
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Detection of prostate cancer related copy number variations with SNP genotyping array
Wang, Y, Yao, X, Li, S-N, Suo, A-L, Tian, T, Ruan, Z-P, Guo, H, Yao, Y
Published in European review for medical and pharmacological sciences (01.11.2013)
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Published in European review for medical and pharmacological sciences (01.11.2013)
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Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene
Clark, Lorraine N., Haamer, Eneli, Mejia-Santana, Helen, Harris, Juliette, Lesage, Suzanne, Durr, Alexandra, Bs, Sabine Janin, Hedrich, Katja, Louis, Elan D., Cote, Lucien J., Andrews, Howard, Fahn, Stanley, Waters, Cheryl, Ford, Blair, Frucht, Steven, Scott, William, Klein, Christine, Brice, Alexis, Roomere, Hanno, Ottman, Ruth, Marder, Karen
Published in Movement disorders (15.05.2007)
Published in Movement disorders (15.05.2007)
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Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage
Belkadi, Aziz, Pedergnana, Vincent, Cobat, Aurélie, Itan, Yuval, Vincent, Quentin B., Abhyankar, Avinash, Shang, Lei, El Baghdadi, Jamila, Bousfiha, Aziz, Alcais, Alexandre, Boisson, Bertrand, Casanova, Jean-Laurent, Abel, Laurent
Published in Proceedings of the National Academy of Sciences - PNAS (14.06.2016)
Published in Proceedings of the National Academy of Sciences - PNAS (14.06.2016)
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Development of highly reliable in silico SNP resource and genotyping assay from exome capture and sequencing: an example from black spruce (Picea mariana)
Pavy, Nathalie, Gagnon, France, Deschênes, Astrid, Boyle, Brian, Beaulieu, Jean, Bousquet, Jean
Published in Molecular ecology resources (01.03.2016)
Published in Molecular ecology resources (01.03.2016)
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A sex-stratified genome-wide association study of tuberculosis using a multi-ethnic genotyping array
Schurz, Haiko, Kinnear, Craig J, Gignoux, Christopher R, Wojcik, Genevieve L, Van Helden, Paul D, Tromp, Gerard C, Henn, Brenna M, Hoal, Eileen G, Moller, Marlo
Published in bioRxiv (31.08.2018)
Published in bioRxiv (31.08.2018)
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Strategies for processing and quality control of Illumina genotyping arrays
Zhao, Shilin, Jing, Wang, Samuels, David C, Sheng, Quanghu, Shyr, Yu, Guo, Yan
Published in Briefings in bioinformatics (28.09.2018)
Published in Briefings in bioinformatics (28.09.2018)
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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Beecham, Ashley H, Patsopoulos, Nikolaos A, Xifara, Dionysia K, Davis, Mary F, Kemppinen, Anu, Cotsapas, Chris, Shah, Tejas S, Spencer, Chris, Booth, David, Goris, An, Oturai, Annette, Saarela, Janna, Fontaine, Bertrand, Hemmer, Bernhard, Martin, Claes, Zipp, Frauke, D'Alfonso, Sandra, Martinelli-Boneschi, Filippo, Taylor, Bruce, Harbo, Hanne F, Kockum, Ingrid, Hillert, Jan, Olsson, Tomas, Ban, Maria, Oksenberg, Jorge R, Hintzen, Rogier, Barcellos, Lisa F, Agliardi, Cristina, Alfredsson, Lars, Alizadeh, Mehdi, Anderson, Carl, Andrews, Robert, Søndergaard, Helle Bach, Baker, Amie, Band, Gavin, Baranzini, Sergio E, Barizzone, Nadia, Barrett, Jeffrey, Bellenguez, Céline, Bergamaschi, Laura, Bernardinelli, Luisa, Berthele, Achim, Biberacher, Viola, Binder, Thomas M C, Blackburn, Hannah, Bomfim, Izaura L, Brambilla, Paola, Broadley, Simon, Brochet, Bruno, Brundin, Lou, Buck, Dorothea, Butzkueven, Helmut, Caillier, Stacy J, Camu, William, Carpentier, Wassila, Cavalla, Paola, Celius, Elisabeth G, Coman, Irène, Comi, Giancarlo, Corrado, Lucia, Cosemans, Leentje, Cournu-Rebeix, Isabelle, Cree, Bruce A C, Cusi, Daniele, Damotte, Vincent, Defer, Gilles, Delgado, Silvia R, Deloukas, Panos, di Sapio, Alessia, Dilthey, Alexander T, Donnelly, Peter, Dubois, Bénédicte, Duddy, Martin, Edkins, Sarah, Elovaara, Irina, Esposito, Federica, Evangelou, Nikos, Fiddes, Barnaby, Field, Judith, Franke, Andre, Freeman, Colin, Frohlich, Irene Y, Galimberti, Daniela, Gieger, Christian, Gourraud, Pierre-Antoine, Graetz, Christiane, Graham, Andrew, Grummel, Verena, Guaschino, Clara, Hadjixenofontos, Athena, Hakonarson, Hakon, Halfpenny, Christopher, Hall, Gillian, Hall, Per, Hamsten, Anders, Harley, James, Harrower, Timothy, Hawkins, Clive, Hellenthal, Garrett, Hillier, Charles
Published in Nature genetics (01.11.2013)
Published in Nature genetics (01.11.2013)
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Genomic characterization of Algerian Guelmoise cattle and their genetic relationship with other North African populations inferred from SNP genotyping arrays
Ben Jemaa, Slim, Rahal, Ourida, Gaouar, Semir Bechir Suheil, Mastrangelo, Salvatore, Boussaha, Mekki, Ciani, Elena
Published in Livestock science (01.11.2018)
Published in Livestock science (01.11.2018)
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Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample
Szatkiewicz, J P, Neale, B M, O'Dushlaine, C, Fromer, M, Goldstein, J I, Moran, J L, Chambert, K, Kähler, A, Magnusson, P K E, Hultman, C M, Sklar, P, Purcell, S, McCarroll, S A, Sullivan, P F
Published in Molecular psychiatry (01.11.2013)
Published in Molecular psychiatry (01.11.2013)
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Genomic characterization of Algerian Guelmoise cattle and their genetic relationship with other North African populations inferred from SNP genotyping arrays
Ben Jemaa, Slim, Rahal, Ourida, Gaouar, Semir Bechir Suheil, Mastrangelo, Salvatore, Boussaha, Mekki, Ciani, Elena
Published in Livestock science (01.11.2018)
Published in Livestock science (01.11.2018)
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An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis
Vassos, Evangelos, Di Forti, Marta, Coleman, Jonathan, Iyegbe, Conrad, Prata, Diana, Euesden, Jack, O’Reilly, Paul, Curtis, Charles, Kolliakou, Anna, Patel, Hamel, Newhouse, Stephen, Traylor, Matthew, Ajnakina, Olesya, Mondelli, Valeria, Marques, Tiago Reis, Gardner-Sood, Poonam, Aitchison, Katherine J., Powell, John, Atakan, Zerrin, Greenwood, Kathryn E., Smith, Shubulade, Ismail, Khalida, Pariante, Carmine, Gaughran, Fiona, Dazzan, Paola, Markus, Hugh S., David, Anthony S., Lewis, Cathryn M., Murray, Robin M., Breen, Gerome
Published in Biological psychiatry (1969) (15.03.2017)
Published in Biological psychiatry (1969) (15.03.2017)
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Complete maternal uniparental isodisomy of chromosome 4 in a subject with major depressive disorder detected by high density SNP genotyping arrays
Middleton, Frank A., Trauzzi, Marco G., Shrimpton, Antony E., Gentile, Karen L., Morley, Christopher P., Medeiros, Helena, Pato, Michele T., Pato, Carlos N.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.01.2006)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.01.2006)
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Two Adjustment Strategies for Imputation across Genotyping Arrays
Xie, Yiran, Hancock, Dana B., Johnson, Eric O., Rice, John P.
Published in Human heredity (01.01.2014)
Published in Human heredity (01.01.2014)
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Genetic risk for schizophrenia and psychosis in Alzheimer disease
DeMichele-Sweet, M A A, Weamer, E A, Klei, L, Vrana, D T, Hollingshead, D J, Seltman, H J, Sims, R, Foroud, T, Hernandez, I, Moreno-Grau, S, Tárraga, L, Boada, M, Ruiz, A, Williams, J, Mayeux, R, Lopez, O L, Sibille, E L, Kamboh, M I, Devlin, B, Sweet, R A
Published in Molecular psychiatry (01.04.2018)
Published in Molecular psychiatry (01.04.2018)
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Genome-Wide Association Study of Copy Number Variants Suggests LTBP1 and FGD4 Are Important for Alcohol Drinking
Pei, Yu-Fang, Zhang, Lei, Yang, Tie-Lin, Han, Yingying, Hai, Rong, Ran, Shu, Tian, Qing, Shen, Hui, Li, Jian, Zhu, Xue-Zhen, Luo, Xingguang, Deng, Hong-Wen
Published in PloS one (25.01.2012)
Published in PloS one (25.01.2012)
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Low-coverage whole-genome sequencing facilitates accurate and cost-effective haplotype reconstruction in complex mouse crosses
Widmayer, Samuel J., Wooldridge, Lydia K., Swanzey, Emily, Barter, Mary, Snow, Chrystal, Saul, Michael, Meng, Qingchang, Dumont, Beth, Reinholdt, Laura, Gatti, Daniel M.
Published in Mammalian genome (01.07.2025)
Published in Mammalian genome (01.07.2025)
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A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism
Book, Adam, Guella, Ilaria, Candido, Tara, Brice, Alexis, Hattori, Nobutaka, Jeon, Beomseok, Farrer, Matthew J.
Published in Frontiers in neurology (11.12.2018)
Published in Frontiers in neurology (11.12.2018)
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