Literature DB >> 29307891

Genetics of kidney diseases in 2017: Unveiling the genetic architecture of kidney disease.

Olivier Devuyst1.   

Abstract

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Year:  2018        PMID: 29307891     DOI: 10.1038/nrneph.2017.177

Source DB:  PubMed          Journal:  Nat Rev Nephrol        ISSN: 1759-5061            Impact factor:   28.314


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  10 in total

Review 1.  Rare inherited kidney diseases: challenges, opportunities, and perspectives.

Authors:  Olivier Devuyst; Nine V A M Knoers; Giuseppe Remuzzi; Franz Schaefer
Journal:  Lancet       Date:  2014-05-24       Impact factor: 79.321

2.  Genomic Disorders and Neurocognitive Impairment in Pediatric CKD.

Authors:  Miguel Verbitsky; Amy J Kogon; Matthew Matheson; Stephen R Hooper; Craig S Wong; Bradley A Warady; Susan L Furth; Ali G Gharavi
Journal:  J Am Soc Nephrol       Date:  2017-03-27       Impact factor: 10.121

Review 3.  Insights into kidney diseases from genome-wide association studies.

Authors:  Matthias Wuttke; Anna Köttgen
Journal:  Nat Rev Nephrol       Date:  2016-08-01       Impact factor: 28.314

4.  Genomic imbalances in pediatric patients with chronic kidney disease.

Authors:  Miguel Verbitsky; Simone Sanna-Cherchi; David A Fasel; Brynn Levy; Krzysztof Kiryluk; Matthias Wuttke; Alison G Abraham; Frederick Kaskel; Anna Köttgen; Bradley A Warady; Susan L Furth; Craig S Wong; Ali G Gharavi
Journal:  J Clin Invest       Date:  2015-04-20       Impact factor: 14.808

5.  Polycystic Kidney Disease without an Apparent Family History.

Authors:  Ioan-Andrei Iliuta; Vinusha Kalatharan; Kairong Wang; Emilie Cornec-Le Gall; John Conklin; Marina Pourafkari; Ryan Ting; Chen Chen; Alessia C Borgo; Ning He; Xuewen Song; Christina M Heyer; Sarah R Senum; Young-Hwan Hwang; Andrew D Paterson; Peter C Harris; Korosh Khalili; York Pei
Journal:  J Am Soc Nephrol       Date:  2017-05-18       Impact factor: 10.121

6.  Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency.

Authors:  Svjetlana Lovric; Sara Goncalves; Heon Yung Gee; Babak Oskouian; Honnappa Srinivas; Won-Il Choi; Shirlee Shril; Shazia Ashraf; Weizhen Tan; Jia Rao; Merlin Airik; David Schapiro; Daniela A Braun; Carolin E Sadowski; Eugen Widmeier; Tilman Jobst-Schwan; Johanna Magdalena Schmidt; Vladimir Girik; Guido Capitani; Jung H Suh; Noëlle Lachaussée; Christelle Arrondel; Julie Patat; Olivier Gribouval; Monica Furlano; Olivia Boyer; Alain Schmitt; Vincent Vuiblet; Seema Hashmi; Rainer Wilcken; Francois P Bernier; A Micheil Innes; Jillian S Parboosingh; Ryan E Lamont; Julian P Midgley; Nicola Wright; Jacek Majewski; Martin Zenker; Franz Schaefer; Navina Kuss; Johann Greil; Thomas Giese; Klaus Schwarz; Vilain Catheline; Denny Schanze; Ingolf Franke; Yves Sznajer; Anne S Truant; Brigitte Adams; Julie Désir; Ronald Biemann; York Pei; Elisabet Ars; Nuria Lloberas; Alvaro Madrid; Vikas R Dharnidharka; Anne M Connolly; Marcia C Willing; Megan A Cooper; Richard P Lifton; Matias Simons; Howard Riezman; Corinne Antignac; Julie D Saba; Friedhelm Hildebrandt
Journal:  J Clin Invest       Date:  2017-02-06       Impact factor: 14.808

7.  Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.

Authors:  Esther Lopez-Rivera; Yangfan P Liu; Miguel Verbitsky; Blair R Anderson; Valentina P Capone; Edgar A Otto; Zhonghai Yan; Adele Mitrotti; Jeremiah Martino; Nicholas J Steers; David A Fasel; Katarina Vukojevic; Rong Deng; Silvia E Racedo; Qingxue Liu; Max Werth; Rik Westland; Asaf Vivante; Gabriel S Makar; Monica Bodria; Matthew G Sampson; Christopher E Gillies; Virginia Vega-Warner; Mariarosa Maiorana; Donald S Petrey; Barry Honig; Vladimir J Lozanovski; Rémi Salomon; Laurence Heidet; Wassila Carpentier; Dominique Gaillard; Alba Carrea; Loreto Gesualdo; Daniele Cusi; Claudia Izzi; Francesco Scolari; Joanna A E van Wijk; Adela Arapovic; Mirna Saraga-Babic; Marijan Saraga; Nenad Kunac; Ali Samii; Donna M McDonald-McGinn; Terrence B Crowley; Elaine H Zackai; Dorota Drozdz; Monika Miklaszewska; Marcin Tkaczyk; Przemyslaw Sikora; Maria Szczepanska; Malgorzata Mizerska-Wasiak; Grazyna Krzemien; Agnieszka Szmigielska; Marcin Zaniew; John M Darlow; Prem Puri; David Barton; Emilio Casolari; Susan L Furth; Bradley A Warady; Zoran Gucev; Hakon Hakonarson; Hana Flogelova; Velibor Tasic; Anna Latos-Bielenska; Anna Materna-Kiryluk; Landino Allegri; Craig S Wong; Iain A Drummond; Vivette D'Agati; Akira Imamoto; Jonathan M Barasch; Friedhelm Hildebrandt; Krzysztof Kiryluk; Richard P Lifton; Bernice E Morrow; Cecile Jeanpierre; Virginia E Papaioannou; Gian Marco Ghiggeri; Ali G Gharavi; Nicholas Katsanis; Simone Sanna-Cherchi
Journal:  N Engl J Med       Date:  2017-01-25       Impact factor: 91.245

8.  Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease.

Authors:  Binu Porath; Vladimir G Gainullin; Emilie Cornec-Le Gall; Elizabeth K Dillinger; Christina M Heyer; Katharina Hopp; Marie E Edwards; Charles D Madsen; Sarah R Mauritz; Carly J Banks; Saurabh Baheti; Bharathi Reddy; José Ignacio Herrero; Jesús M Bañales; Marie C Hogan; Velibor Tasic; Terry J Watnick; Arlene B Chapman; Cécile Vigneau; Frédéric Lavainne; Marie-Pierre Audrézet; Claude Ferec; Yannick Le Meur; Vicente E Torres; Peter C Harris
Journal:  Am J Hum Genet       Date:  2016-06-02       Impact factor: 11.025

9.  A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.

Authors:  Carolin E Sadowski; Svjetlana Lovric; Shazia Ashraf; Werner L Pabst; Heon Yung Gee; Stefan Kohl; Susanne Engelmann; Virginia Vega-Warner; Humphrey Fang; Jan Halbritter; Michael J Somers; Weizhen Tan; Shirlee Shril; Inès Fessi; Richard P Lifton; Detlef Bockenhauer; Sherif El-Desoky; Jameela A Kari; Martin Zenker; Markus J Kemper; Dominik Mueller; Hanan M Fathy; Neveen A Soliman; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2014-10-27       Impact factor: 10.121

10.  Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome.

Authors:  Rathi Prasad; Irene Hadjidemetriou; Avinaash Maharaj; Eirini Meimaridou; Federica Buonocore; Moin Saleem; Jenny Hurcombe; Agnieszka Bierzynska; Eliana Barbagelata; Ignacio Bergadá; Hamilton Cassinelli; Urmi Das; Ruth Krone; Bulent Hacihamdioglu; Erkan Sari; Ediz Yesilkaya; Helen L Storr; Maria Clemente; Monica Fernandez-Cancio; Nuria Camats; Nanik Ram; John C Achermann; Paul P Van Veldhoven; Leonardo Guasti; Debora Braslavsky; Tulay Guran; Louise A Metherell
Journal:  J Clin Invest       Date:  2017-02-06       Impact factor: 14.808

  10 in total
  4 in total

1.  Genome-Wide Association Studies of CKD and Related Traits.

Authors:  Adrienne Tin; Anna Köttgen
Journal:  Clin J Am Soc Nephrol       Date:  2020-05-14       Impact factor: 8.237

2.  The Ion Channel-Related Gene Signatures Correlated With Diagnosis, Prognosis, and Individualized Treatment in Patients With Clear Cell Renal Cell Carcinoma.

Authors:  Zhenpeng Zhu; Zhenchuan Lei; Jinqin Qian; Cuijian Zhang; Yanqing Gong; Guicao Yin; Yifan Li; Xuesong Li; Jian Lin; Liqun Zhou
Journal:  Front Pharmacol       Date:  2022-06-01       Impact factor: 5.988

3.  Ganab Haploinsufficiency Does Not Cause Polycystic Kidney Disease or Polycystic Liver Disease in Mice.

Authors:  Guangrui Geng; Yunming Xiao; Yingjie Zhang; Wanjun Shen; Jiaona Liu; Fei Zhu; Xu Wang; Jie Wu; Ran Liu; Guangyan Cai; Xueyuan Bai; Qinggang Li; Xiangmei Chen
Journal:  Biomed Res Int       Date:  2020-05-19       Impact factor: 3.411

Review 4.  How Genetics Can Improve Clinical Practice in Chronic Kidney Disease: From Bench to Bedside.

Authors:  Doloretta Piras; Nicola Lepori; Gianfranca Cabiddu; Antonello Pani
Journal:  J Pers Med       Date:  2022-01-31
  4 in total

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