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Number of items: 10.

2016

Morris, David L., Sheng, Yujun, Zhang, Yan, Wang, Yong-Fei, Zhu, Zhengwei, Tombleson, Philip, Chen, Lingyan, Graham, Deborah S. Cunninghame, Bentham, James, Roberts, Amy L., and others. (2016) Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. Nature Genetics, 48 . pp. 940-946. ISSN 1061-4036. E-ISSN 1546-1718. (doi:10.1038/ng.3603) (KAR id:64442)

Redin, Claire, Brand, Harrison, Collins, Ryan L, Kammin, Tammy, Mitchell, Elyse, Hodge, Jennelle C, Hanscom, Carrie, Pillalamarri, Vamsee, Seabra, Catarina M, Abbott, Mary-Alice, and others. (2016) The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nature Genetics, 49 (1). pp. 36-45. ISSN 1061-4036. (doi:10.1038/ng.3720) (KAR id:81265)

2015

Bentham, James, Morris, David L, Cunninghame Graham, Deborah S, Pinder, Christopher L, Tombleson, Philip, Behrens, Timothy W, Martín, Javier, Fairfax, Benjamin P, Knight, Julian C, Chen, Lingyan, and others. (2015) Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. Nature Genetics, 47 (12). pp. 1457-1464. ISSN 1061-4036. (doi:10.1038/ng.3434) (KAR id:64033)

Ottolini, Christian S, Newnham, Louise J, Capalbo, Antonio, Natesan, Senthilkumar A, Joshi, Hrishikesh A, Cimadomo, Danilo, Griffin, Darren K., Sage, Karen, Summers, Michael C, Thornhill, Alan R, and others. (2015) Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates. Nature Genetics, 47 (7). pp. 727-735. ISSN 1061-4036. (doi:10.1038/ng.3306) (KAR id:59356)

2013

Huang, Yinhua, Li, Yingrui, Burt, David W., Chen, Hualan, Zhang, Yong, Qian, Wubin, Kim, Heebal, Gan, Shangquan, Zhao, Yiqiang, Li, Jianwen, and others. (2013) The duck genome and transcriptome provide insight into an avian influenza virus reservoir species. Nature Genetics, 45 (7). pp. 776-783. ISSN 1061-4036. (doi:10.1038/ng.2657) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:41101)

2011

Chambers, John C, Zhang, Weihua, Sehmi, Joban S., Li, Xinzhong, Wass, Mark N., Van der Harst, Pim, Holm, Hilma, Sanna, Serena, Kavousi, Maryam, Baumeister, Sebastian E, and others. (2011) Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nature Genetics, 43 (11). pp. 1131-1138. ISSN 1061-4036. (doi:10.1038/ng.970) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:34217)

2010

Chambers, John C, Zhang, Weihua, Lord, Graham M, van der Harst, Pim, Lawlor, Debbie A, Sehmi, Joban S., Gale, Daniel P, Wass, Mark N., Ahmadi, Kourosh R, Bakker, Stephan J L, and others. (2010) Genetic loci influencing kidney function and chronic kidney disease. Nature Genetics, 42 (5). pp. 373-5. ISSN 1061-4036. (doi:10.1038/ng.566) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:34185)

Chambers, John C, Zhao, Jing, Terracciano, Cesare M.N., Bezzina, Connie R., Zhang, Weihua, Kaba, Riyaz, Navaratnarajah, Manoraj, Lotlikar, Amol, Sehmi, Joban S., Kooner, Manraj K., and others. (2010) Genetic variation in SCN10A influences cardiac conduction. Nature Genetics, 42 (2). pp. 149-152. ISSN 1546-1718. (doi:10.1038/ng.516) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:34181)

2009

Chambers, John C, Zhang, Weihua, Li, Yun, Sehmi, Joban S., Wass, Mark N., Zabaneh, Delilah, Hoggart, Clive, Bayele, Henry, McCarthy, Mark I, Peltonen, Leena, and others. (2009) Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. Nature Genetics, 41 (11). pp. 1170-1172. ISSN 1061-4036. (doi:10.1038/ng.462) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:34184)

2000

Hong, Susan E., Shugart, Yin Yao, Huang, David T., Shahwan, Saad Al, Grant, P. Ellen, Hourihane, Jonathan O'B, Martin, Neil D. T., Walsh, Christopher A. (2000) Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nature Genetics, 26 (1). pp. 93-96. ISSN 1061-4036. (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:16231)

This list was generated on Sat Oct 19 23:16:30 2024 BST.