Literature DB >> 33664247

Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families.

Hope A Tanudisastro1, Katherine Holman2,3, Gladys Ho2,3,4, Elizabeth Farnsworth2,3, Katrina Fisk2, Thet Gayagay2, Emma Hackett2, Gemma Jenkins2, Rahul Krishnaraj2, Tiffany Lai2, Karen Wong2, Chirag Patel3,5, Amali Mallawaarachchi3,6,7, Andrew J Mallett3,8,9, Bruce Bennetts2,3,4, Stephen I Alexander10,11,12, Hugh J McCarthy13,14,15.   

Abstract

Genetic testing in nephrology clinical practice has moved rapidly from a rare specialized test to routine practice both in pediatric and adult nephrology. However, clear information pertaining to the likely outcome of testing is still missing. Here we describe the experience of the accredited Australia and New Zealand Renal Gene Panels clinical service, reporting on sequencing for 552 individuals from 542 families with suspected kidney disease in Australia and New Zealand. An increasing number of referrals have been processed since service inception with an overall diagnostic rate of 35%. The likelihood of identifying a causative variant varies according to both age at referral and gene panel. Although results from high throughput genetic testing have been primarily for diagnostic purposes, they will increasingly play an important role in directing treatment, genetic counseling, and family planning.

Entities:  

Year:  2021        PMID: 33664247      PMCID: PMC7933190          DOI: 10.1038/s41525-021-00184-x

Source DB:  PubMed          Journal:  NPJ Genom Med        ISSN: 2056-7944            Impact factor:   8.617


  55 in total

Review 1.  Molecular diagnostics for autosomal dominant polycystic kidney disease.

Authors:  Peter C Harris; Sandro Rossetti
Journal:  Nat Rev Nephrol       Date:  2010-02-23       Impact factor: 28.314

2.  Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.

Authors:  Natasha T Strande; Erin Rooney Riggs; Adam H Buchanan; Ozge Ceyhan-Birsoy; Marina DiStefano; Selina S Dwight; Jenny Goldstein; Rajarshi Ghosh; Bryce A Seifert; Tam P Sneddon; Matt W Wright; Laura V Milko; J Michael Cherry; Monica A Giovanni; Michael F Murray; Julianne M O'Daniel; Erin M Ramos; Avni B Santani; Alan F Scott; Sharon E Plon; Heidi L Rehm; Christa L Martin; Jonathan S Berg
Journal:  Am J Hum Genet       Date:  2017-05-25       Impact factor: 11.025

3.  Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes.

Authors:  Asli Ece Solmaz; Huseyin Onay; Tahir Atik; Ayca Aykut; Meltem Cerrah Gunes; Ozge Ozalp Yuregir; Veysel Nijat Bas; Filiz Hazan; Ozgur Kirbiyik; Ferda Ozkinay
Journal:  Eur J Med Genet       Date:  2015-10-27       Impact factor: 2.708

4.  Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis.

Authors:  Daniela Anne Braun; Jennifer Ashley Lawson; Heon Yung Gee; Jan Halbritter; Shirlee Shril; Weizhen Tan; Deborah Stein; Ari J Wassner; Michael A Ferguson; Zoran Gucev; Brittany Fisher; Leslie Spaneas; Jennifer Varner; John A Sayer; Danko Milosevic; Michelle Baum; Velibor Tasic; Friedhelm Hildebrandt
Journal:  Clin J Am Soc Nephrol       Date:  2016-01-19       Impact factor: 8.237

5.  Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin.

Authors:  Arif B Ekici; Thomas Hackenbeck; Vincent Morinière; Andrea Pannes; Maike Buettner; Steffen Uebe; Rolf Janka; Antje Wiesener; Ingo Hermann; Sina Grupp; Martin Hornberger; Tobias B Huber; Nikky Isbel; George Mangos; Stella McGinn; Daniela Soreth-Rieke; Bodo B Beck; Michael Uder; Kerstin Amann; Corinne Antignac; André Reis; Kai-Uwe Eckardt; Michael S Wiesener
Journal:  Kidney Int       Date:  2014-03-26       Impact factor: 10.612

Review 6.  CRISPR/Cas9 technology as a potent molecular tool for gene therapy.

Authors:  Ansar Karimian; Khalil Azizian; Hadi Parsian; Sona Rafieian; Vahid Shafiei-Irannejad; Maryam Kheyrollah; Mehdi Yousefi; Maryam Majidinia; Bahman Yousefi
Journal:  J Cell Physiol       Date:  2019-01-30       Impact factor: 6.384

7.  Evidence of digenic inheritance in Alport syndrome.

Authors:  Maria Antonietta Mencarelli; Laurence Heidet; Helen Storey; Michel van Geel; Bertrand Knebelmann; Chiara Fallerini; Nunzia Miglietti; Maria Fatima Antonucci; Francesco Cetta; John A Sayer; Arthur van den Wijngaard; Shu Yau; Francesca Mari; Mirella Bruttini; Francesca Ariani; Karin Dahan; Bert Smeets; Corinne Antignac; Frances Flinter; Alessandra Renieri
Journal:  J Med Genet       Date:  2015-01-09       Impact factor: 6.318

8.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

Review 9.  Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.

Authors:  Valentina P Capone; William Morello; Francesca Taroni; Giovanni Montini
Journal:  Int J Mol Sci       Date:  2017-04-11       Impact factor: 5.923

10.  Analysis of protein-coding genetic variation in 60,706 humans.

Authors:  Monkol Lek; Konrad J Karczewski; Eric V Minikel; Kaitlin E Samocha; Eric Banks; Timothy Fennell; Anne H O'Donnell-Luria; James S Ware; Andrew J Hill; Beryl B Cummings; Taru Tukiainen; Daniel P Birnbaum; Jack A Kosmicki; Laramie E Duncan; Karol Estrada; Fengmei Zhao; James Zou; Emma Pierce-Hoffman; Joanne Berghout; David N Cooper; Nicole Deflaux; Mark DePristo; Ron Do; Jason Flannick; Menachem Fromer; Laura Gauthier; Jackie Goldstein; Namrata Gupta; Daniel Howrigan; Adam Kiezun; Mitja I Kurki; Ami Levy Moonshine; Pradeep Natarajan; Lorena Orozco; Gina M Peloso; Ryan Poplin; Manuel A Rivas; Valentin Ruano-Rubio; Samuel A Rose; Douglas M Ruderfer; Khalid Shakir; Peter D Stenson; Christine Stevens; Brett P Thomas; Grace Tiao; Maria T Tusie-Luna; Ben Weisburd; Hong-Hee Won; Dongmei Yu; David M Altshuler; Diego Ardissino; Michael Boehnke; John Danesh; Stacey Donnelly; Roberto Elosua; Jose C Florez; Stacey B Gabriel; Gad Getz; Stephen J Glatt; Christina M Hultman; Sekar Kathiresan; Markku Laakso; Steven McCarroll; Mark I McCarthy; Dermot McGovern; Ruth McPherson; Benjamin M Neale; Aarno Palotie; Shaun M Purcell; Danish Saleheen; Jeremiah M Scharf; Pamela Sklar; Patrick F Sullivan; Jaakko Tuomilehto; Ming T Tsuang; Hugh C Watkins; James G Wilson; Mark J Daly; Daniel G MacArthur
Journal:  Nature       Date:  2016-08-18       Impact factor: 49.962

View more
  2 in total

1.  A clinical approach to tubulopathies in children and young adults.

Authors:  Andrew Mallett; Hugh McCarthy; Rachael Kermond
Journal:  Pediatr Nephrol       Date:  2022-05-18       Impact factor: 3.714

Review 2.  Best practices for the interpretation and reporting of clinical whole genome sequencing.

Authors:  Christina A Austin-Tse; Vaidehi Jobanputra; Hutton M Kearney; Heidi L Rehm; Denise L Perry; David Bick; Ryan J Taft; Eric Venner; Richard A Gibbs; Ted Young; Sarah Barnett; John W Belmont; Nicole Boczek; Shimul Chowdhury; Katarzyna A Ellsworth; Saurav Guha; Shashikant Kulkarni; Cherisse Marcou; Linyan Meng; David R Murdock; Atteeq U Rehman; Elizabeth Spiteri; Amanda Thomas-Wilson
Journal:  NPJ Genom Med       Date:  2022-04-08       Impact factor: 6.083

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.