Journal: Genetical research - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Journal Genetical research

1. A de novo microdeletion in NRXN1 in a Dutch patient with mild intellectual disability, microcephaly and gonadal dysgenesis. (6th October 2015)

Authors:: AGHA, ZEHRA; IQBAL, ZAFAR; KLEEFSTRA, TJITSKE; ZWEIER, CHRISTIANE; PFUNDT, ROLPH; QAMAR, RAHEEL; VAN BOKHOVEN, HANS; WILLEMSEN, MARJOLEIN H.
Journal:: Genetical research
Issue:: Volume 97(2015)
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Record Type:: Journal Article
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2. A nonparametric method to test for associations between rare variants and multiple traits. (2016)

Authors:: ZHOU, YING; CHENG, YANGYANG; ZHU, WENSHENG; ZHOU, QIAN
Journal:: Genetical research
Issue:: Volume 98(2016)
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Record Type:: Journal Article
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3. A permutation method for detecting trend correlations in rare variant association studies. (2019)

Authors:: Liu, Lifeng; Wang, Pengfei; Meng, Jingbo; Chen, Lili; Zhu, Wensheng; Ma, Weijun
Journal:: Genetical research
Issue:: Volume 101(2019)
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Record Type:: Journal Article
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4. A refined high carbohydrate diet is associated with changes in the serotonin pathway and visceral obesity. (28th December 2015)

Authors:: SPADARO, PAOLA A.; NAUG, HELEN L.; DU TOIT, EUGENE F.; DONNER, DANIEL; COLSON, NATALIE J.
Journal:: Genetical research
Issue:: Volume 97(2015)
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Record Type:: Journal Article
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5. A robust test for X-chromosome genetic association accounting for X-chromosome inactivation and imprinting. (2020)

Authors:: Zhang, Yu; Xu, Si-Qi; Liu, Wei; Fung, Wing Kam; Zhou, Ji-Yuan
Journal:: Genetical research
Issue:: Volume 102(2020)
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Record Type:: Journal Article
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6. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. (2019)

Authors:: Jaouadi, Hager; Chehida, Amel Ben; Kraoua, Lilia; Etchevers, Heather C.; Argiro, Laurent; Kasdallah, Nadia; Blibech, Sonia; Delague, Valérie; Lévy, Nicolas; Tebib, Néji; Mrad, Ridha; Abdelhak, Sonia; Benkhalifa, Rym; Zaffran, Stéphane
Journal:: Genetical research
Issue:: Volume 101(2019)
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Record Type:: Journal Article
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7. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. (29th April 2019)

Authors:: Jaouadi, Hager; Chehida, Amel Ben; Kraoua, Lilia; Etchevers, Heather C.; Argiro, Laurent; Kasdallah, Nadia; Blibech, Sonia; Delague, Valérie; Lévy, Nicolas; Tebib, Néji; Mrad, Ridha; Abdelhak, Sonia; Benkhalifa, Rym; Zaffran, Stéphane
Journal:: Genetical research
Issue:: Volume 101(2019)
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Record Type:: Journal Article
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8. A Survival Model Based on the ASB Genes and Used to Predict the Prognosis of Kidney Renal Clear Cell Carcinoma. (22nd February 2023)

Authors:: Xie, Deqian; Dai, Lu; Yang, Xiaolei; Huang, Tao; Zheng, Wei
Other Names:: Ruan Ningke Academic Editor.
Journal:: Genetical research
Issue:: Volume 2023(2023)
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Record Type:: Journal Article
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9. A unified approach to characterize and conserve adaptive and neutral genetic diversity in subdivided populations. (16th December 2014)

Authors:: WELLMANN, ROBIN; BENNEWITZ, JÖRN; MEUWISSEN, THEO H. E.
Journal:: Genetical research
Issue:: Volume 96(2014)
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Record Type:: Journal Article
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10. ABIN1 Inhibits Inflammation through Necroptosis-Dependent Pathway in Ulcerative Colitis. (8th August 2022)

Authors:: Bao, Jing; Ye, Bin; Ren, Yuhan
Other Names:: Yang Jun Academic Editor.
Journal:: Genetical research
Issue:: Volume 2022(2022)
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Record Type:: Journal Article
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