Literature DB >> 27925785

Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health-NHLBI Workshop, September 3 and 4, 2015.

Lisa R Young1, Bruce C Trapnell2,3, Kenneth D Mandl4,5, Daniel T Swarr6, Jennifer A Wambach7, Carol J Blaisdell8.   

Abstract

Pediatric rare lung disease (PRLD) is a term that refers to a heterogeneous group of rare disorders in children. In recent years, this field has experienced significant progress marked by scientific discoveries, multicenter and interdisciplinary collaborations, and efforts of patient advocates. Although genetic mechanisms underlie many PRLDs, pathogenesis remains uncertain for many of these disorders. Furthermore, epidemiology and natural history are insufficiently defined, and therapies are limited. To develop strategies to accelerate scientific advancement for PRLD research, the NHLBI of the National Institutes of Health convened a strategic planning workshop on September 3 and 4, 2015. The workshop brought together a group of scientific experts, intramural and extramural investigators, and advocacy groups with the following objectives: (1) to discuss the current state of PRLD research; (2) to identify scientific gaps and barriers to increasing research and improving outcomes for PRLDs; (3) to identify technologies, tools, and reagents that could be leveraged to accelerate advancement of research in this field; and (4) to develop priorities for research aimed at improving patient outcomes and quality of life. This report summarizes the workshop discussion and provides specific recommendations to guide future research in PRLD.

Entities:  

Keywords:  children; discovery; genomics; outcomes; rare disease

Mesh:

Year:  2016        PMID: 27925785      PMCID: PMC5291498          DOI: 10.1513/AnnalsATS.201605-402OT

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


  43 in total

1.  A mutation in the surfactant protein C gene associated with familial interstitial lung disease.

Authors:  L M Nogee; A E Dunbar; S E Wert; F Askin; A Hamvas; J A Whitsett
Journal:  N Engl J Med       Date:  2001-02-22       Impact factor: 91.245

2.  Strategies for maintaining patient privacy in i2b2.

Authors:  Shawn N Murphy; Vivian Gainer; Michael Mendis; Susanne Churchill; Isaac Kohane
Journal:  J Am Med Inform Assoc       Date:  2011-10-07       Impact factor: 4.497

3.  Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype.

Authors:  Stephanie D Davis; Thomas W Ferkol; Margaret Rosenfeld; Hye-Seung Lee; Sharon D Dell; Scott D Sagel; Carlos Milla; Maimoona A Zariwala; Jessica E Pittman; Adam J Shapiro; Johnny L Carson; Jeffrey P Krischer; Milan J Hazucha; Matthew L Cooper; Michael R Knowles; Margaret W Leigh
Journal:  Am J Respir Crit Care Med       Date:  2015-02-01       Impact factor: 21.405

4.  Federalist principles for healthcare data networks.

Authors:  Kenneth D Mandl; Isaac S Kohane
Journal:  Nat Biotechnol       Date:  2015-04       Impact factor: 54.908

5.  Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.

Authors:  Sara M Sarasua; Luigi Boccuto; Julia L Sharp; Alka Dwivedi; Chin-Fu Chen; Jonathan D Rollins; R Curtis Rogers; Katy Phelan; Barbara R DuPont
Journal:  Hum Genet       Date:  2014-01-31       Impact factor: 4.132

6.  Identification of the cystic fibrosis gene: chromosome walking and jumping.

Authors:  J M Rommens; M C Iannuzzi; B Kerem; M L Drumm; G Melmer; M Dean; R Rozmahel; J L Cole; D Kennedy; N Hidaka
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

7.  Human GM-CSF autoantibodies and reproduction of pulmonary alveolar proteinosis.

Authors:  Takuro Sakagami; Kanji Uchida; Takuji Suzuki; Brenna C Carey; Robert E Wood; Susan E Wert; Jeffrey A Whitsett; Bruce C Trapnell; Maurizio Luisetti
Journal:  N Engl J Med       Date:  2009-12-31       Impact factor: 91.245

8.  Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

Authors:  Takuji Suzuki; Takuro Sakagami; Bruce K Rubin; Lawrence M Nogee; Robert E Wood; Sarah L Zimmerman; Teresa Smolarek; Megan K Dishop; Susan E Wert; Jeffrey A Whitsett; Gregory Grabowski; Brenna C Carey; Carrie Stevens; Johannes C M van der Loo; Bruce C Trapnell
Journal:  J Exp Med       Date:  2008-10-27       Impact factor: 14.307

9.  Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1.

Authors:  Margarita Martinez-Moczygemba; Minh L Doan; Okan Elidemir; Leland L Fan; Sau Wai Cheung; Jonathan T Lei; James P Moore; Ghamartaj Tavana; Lora R Lewis; Yiming Zhu; Donna M Muzny; Richard A Gibbs; David P Huston
Journal:  J Exp Med       Date:  2008-10-27       Impact factor: 14.307

10.  tranSMART: An Open Source and Community-Driven Informatics and Data Sharing Platform for Clinical and Translational Research.

Authors:  Brian D Athey; Michael Braxenthaler; Magali Haas; Yike Guo
Journal:  AMIA Jt Summits Transl Sci Proc       Date:  2013-03-18
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  4 in total

1.  Pulmonary Aptamer Signatures in Children's Interstitial and Diffuse Lung Disease.

Authors:  Robin R Deterding; Brandie D Wagner; J Kirk Harris; Emily M DeBoer
Journal:  Am J Respir Crit Care Med       Date:  2019-12-15       Impact factor: 21.405

2.  Identifying Biomarkers in Pediatric Rare Lung Disease. chILD Grows Up.

Authors:  Timothy J Vece; Charles R Esther
Journal:  Am J Respir Crit Care Med       Date:  2019-12-15       Impact factor: 21.405

3.  Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung Transplantation.

Authors:  Christopher T Towe; Frances V White; R Mark Grady; Stuart C Sweet; Pirooz Eghtesady; Daniel J Wegner; Partha Sen; Przemyslaw Szafranski; Pawel Stankiewicz; Aaron Hamvas; F Sessions Cole; Jennifer A Wambach
Journal:  J Pediatr       Date:  2017-12-01       Impact factor: 4.406

4.  Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype.

Authors:  Dan Dai; Mei Mei; Liyuan Hu; Yun Cao; Xiaochuan Wang; Libo Wang; Yulan Lu; Lin Yang; Xinran Dong; Huijun Wang; Bingbing Wu; Liling Qian
Journal:  Arch Dis Child       Date:  2021-06-16       Impact factor: 3.791

  4 in total

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