Literature DB >> 27510613

Editorial: New Horizons in Genetic Diagnosis in Pediatric Practice: The Excitement and Challenges!

Ratna D Puri1, Madhulika Kabra2.   

Abstract

Year:  2016        PMID: 27510613     DOI: 10.1007/s12098-016-2204-1

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


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  8 in total

Review 1.  When to Suspect and How to Diagnose Mitochondrial Disorders?

Authors:  Sergei Korenev; Andrew A M Morris
Journal:  Indian J Pediatr       Date:  2016-01-13       Impact factor: 1.967

Review 2.  Genetic diagnosis and testing in clinical practice.

Authors:  Elizabeth McPherson
Journal:  Clin Med Res       Date:  2006-06

3.  Genetic Studies in Autism.

Authors:  Shruthi Sudarshan; Neerja Gupta; Madhulika Kabra
Journal:  Indian J Pediatr       Date:  2016-03-03       Impact factor: 1.967

4.  Genetic Approach to Diagnosis of Intellectual Disability.

Authors:  Ratna Dua Puri; Moni Tuteja; I C Verma
Journal:  Indian J Pediatr       Date:  2016-09-13       Impact factor: 1.967

Review 5.  Advances in the Understanding of the Genetic Causes of Hearing Loss in Children Inform a Rational Approach to Evaluation.

Authors:  John C Carey; Janice C Palumbos
Journal:  Indian J Pediatr       Date:  2016-01-08       Impact factor: 1.967

Review 6.  Molecular genetic testing and the future of clinical genomics.

Authors:  Sara Huston Katsanis; Nicholas Katsanis
Journal:  Nat Rev Genet       Date:  2013-06       Impact factor: 53.242

Review 7.  Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.

Authors:  Jaina Patel; Saadet Mercimek-Mahmutoglu
Journal:  Indian J Pediatr       Date:  2016-01-29       Impact factor: 1.967

8.  Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.

Authors:  Dimitri J Stavropoulos; Daniele Merico; Rebekah Jobling; Sarah Bowdin; Nasim Monfared; Bhooma Thiruvahindrapuram; Thomas Nalpathamkalam; Giovanna Pellecchia; Ryan K C Yuen; Michael J Szego; Robin Z Hayeems; Randi Zlotnik Shaul; Michael Brudno; Marta Girdea; Brendan Frey; Babak Alipanahi; Sohnee Ahmed; Riyana Babul-Hirji; Ramses Badilla Porras; Melissa T Carter; Lauren Chad; Ayeshah Chaudhry; David Chitayat; Soghra Jougheh Doust; Cheryl Cytrynbaum; Lucie Dupuis; Resham Ejaz; Leona Fishman; Andrea Guerin; Bita Hashemi; Mayada Helal; Stacy Hewson; Michal Inbar-Feigenberg; Peter Kannu; Natalya Karp; Raymond Kim; Jonathan Kronick; Eriskay Liston; Heather MacDonald; Saadet Mercimek-Mahmutoglu; Roberto Mendoza-Londono; Enas Nasr; Graeme Nimmo; Nicole Parkinson; Nada Quercia; Julian Raiman; Maian Roifman; Andreas Schulze; Andrea Shugar; Cheryl Shuman; Pierre Sinajon; Komudi Siriwardena; Rosanna Weksberg; Grace Yoon; Chris Carew; Raith Erickson; Richard A Leach; Robert Klein; Peter N Ray; M Stephen Meyn; Stephen W Scherer; Ronald D Cohn; Christian R Marshall
Journal:  NPJ Genom Med       Date:  2016-01-13       Impact factor: 8.617

  8 in total
  1 in total

Review 1.  Genomics of rare genetic diseases-experiences from India.

Authors:  Sridhar Sivasubbu; Vinod Scaria
Journal:  Hum Genomics       Date:  2019-09-25       Impact factor: 4.639

  1 in total

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