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CORC

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The copy number variation landscape of congenital anomalies of the kidney and urinary tract 期刊论文
NATURE GENETICS, 2019, 卷号: 51, 期号: 1
作者:  Verbitsky, Miguel;  Westland, Rik;  Perez, Alejandra;  Kiryluk, Krzysztof;  Liu, Qingxue
收藏  |  浏览/下载：21/0  |  提交时间：2019/12/05
The copy number variation landscape of congenital anomalies of the kidney and urinary tract 期刊论文
2019, 卷号: 51, 期号: 1, 页码: 117-+
作者:  Verbitsky, Miguel;  Westland, Rik;  Perez, Alejandra;  Kiryluk, Krzysztof;  Liu, Qingxue
收藏  |  浏览/下载：28/0  |  提交时间：2020/01/03
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics 期刊论文
2018, 卷号: 27, 期号: [db:dc_citation_issue], 页码: 742
作者:  Beaumont, Robin N.[1];  Warrington, Nicole M.[2];  Cavadino, Alana[3];  Tyrrell, Jessica[1,4];  Nodzenski, Michael[5]
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/03
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains 期刊论文
Nature Neuroscience, 2017, 卷号: 20, 期号: 8, 页码: 1043-1051
作者:  Geisheker, Madeleine R.;  Heymann, Gabriel;  Wang, Tianyun;  Coe, Bradley P.;  Turner, Tychele N.
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/03
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight 期刊论文
2016, 卷号: 315, 期号: [db:dc_citation_issue], 页码: 1129
作者:  Tyrrell, Jessica[3,4];  Richmond, Rebecca C.[5,6,7];  Palmer, Tom M.[8,9];  Feenstra, Bjarke[10];  Rangarajan, Janani[11]
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/03
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight 期刊论文
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 卷号: 315, 页码: 1129-1140
作者:  Tyrrell, Jessica[3,4];  Richmond, Rebecca C.[5,6,7];  Palmer, Tom M.[8,9];  Feenstra, Bjarke[10];  Rangarajan, Janani[11]
收藏  |  浏览/下载：10/0  |  提交时间：2019/04/24
A novel common variant in DCST2 is associated with length in early life and height in adulthood 期刊论文
2015, 卷号: 24, 期号: [db:dc_citation_issue], 页码: 1155
作者:  van der Valk, Ralf J. P.[1,2,3];  Kreiner-Moller, Eskil[5,6];  Kooijman, Marjolein N.[1,2,3];  Guxens, Monica[7,8,9];  Stergiakouli, Evangelia[10]
收藏  |  浏览/下载：27/0  |  提交时间：2019/12/03
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia 期刊论文
HUMAN MOLECULAR GENETICS, 2015, 卷号: 24, 期号: 8
作者:  Menezes, Minal J.;  Guo, Yiran;  Zhang, Jianguo;  Riley, Lisa G.;  Cooper, Sandra T.
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/19
Copy Number Variation on Chromosome 10q26.3 for Obesity Identified by a Genome-Wide Study 期刊论文
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 卷号: 98, 期号: [db:dc_citation_issue], 页码: E191-E195
作者:  Yang, Tie-Lin;  Guo, Yan;  Shen, Hui;  Li, Jian;  Glessner, Joseph T.
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/10
METHOD OF DIAGNOSIS AND TREATMENT FOR ASTHMA BASED ON HAPLOTYPE ASSOCIATION 专利
作者:  HALAPI EVA;  HAKONARSON HAKON;  GURNEY MARK E
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05

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