Literature DB >> 26846157

The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine.

William A Gahl1, John J Mulvihill2, Camilo Toro1, Thomas C Markello1, Anastasia L Wise1, Rachel B Ramoni3, David R Adams1, Cynthia J Tifft1.   

Abstract

INTRODUCTION: The inability of some seriously and chronically ill individuals to receive a definitive diagnosis represents an unmet medical need. In 2008, the NIH Undiagnosed Diseases Program (UDP) was established to provide answers to patients with mysterious conditions that long eluded diagnosis and to advance medical knowledge. Patients admitted to the NIH UDP undergo a five-day hospitalization, facilitating highly collaborative clinical evaluations and a detailed, standardized documentation of the individual's phenotype. Bedside and bench investigations are tightly coupled. Genetic studies include commercially available testing, single nucleotide polymorphism microarray analysis, and family exomic sequencing studies. Selected gene variants are evaluated by collaborators using informatics, in vitro cell studies, and functional assays in model systems (fly, zebrafish, worm, or mouse). INSIGHTS FROM THE UDP: In seven years, the UDP received 2954 complete applications and evaluated 863 individuals. Nine vignettes (two unpublished) illustrate the relevance of an undiagnosed diseases program to complex and common disorders, the coincidence of multiple rare single gene disorders in individual patients, newly recognized mechanisms of disease, and the application of precision medicine to patient care.
CONCLUSIONS: The UDP provides examples of the benefits expected to accrue with the recent launch of a national Undiagnosed Diseases Network (UDN). The UDN should accelerate rare disease diagnosis and new disease discovery, enhance the likelihood of diagnosing known diseases in patients with uncommon phenotypes, improve management strategies, and advance medical research. Published by Elsevier Inc.

Entities:  

Keywords:  Exome sequencing; Interdisciplinary research; Precision medicine; Undiagnosed and rare diseases

Mesh:

Year:  2016        PMID: 26846157      PMCID: PMC5560125          DOI: 10.1016/j.ymgme.2016.01.007

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  60 in total

1.  MED23-associated intellectual disability in a non-consanguineous family.

Authors:  Aditi Trehan; Jacqueline M Brady; Valerie Maduro; William P Bone; Yan Huang; Gretchen A Golas; Megan S Kane; Paul R Lee; Audrey Thurm; Andrea L Gropman; Scott M Paul; Gilbert Vezina; Thomas C Markello; William A Gahl; Cornelius F Boerkoel; Cynthia J Tifft
Journal:  Am J Med Genet A       Date:  2015-04-02       Impact factor: 2.802

2.  ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination.

Authors:  Laila Shehata; Dimitre R Simeonov; Anja Raams; Lynne Wolfe; Adeline Vanderver; Xueli Li; Yan Huang; Shannon Garner; Cornelius F Boerkoel; Audrey Thurm; Gail E Herman; Cynthia J Tifft; Miao He; Nicolaas G J Jaspers; William A Gahl
Journal:  Am J Med Genet A       Date:  2014-09-22       Impact factor: 2.802

3.  Neurotransmitter abnormalities and response to supplementation in SPG11.

Authors:  Adeline Vanderver; Davide Tonduti; Sarah Auerbach; Johanna L Schmidt; Sumit Parikh; Gordon C Gowans; Kelly E Jackson; Pamela L Brock; Marc Patterson; Michelle Nehrebecky; Rena Godfrey; Wadih M Zein; William Gahl; Camilo Toro
Journal:  Mol Genet Metab       Date:  2012-06-01       Impact factor: 4.797

4.  A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency.

Authors:  G J Gerwig; E Bause; L K Nuytinck; J F Vliegenthart; W Breuer; J P Kamerling; M F Espeel; J J Martin; N W Chan; G A Dacremont
Journal:  Am J Hum Genet       Date:  2000-04-28       Impact factor: 11.025

5.  Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.

Authors:  Shannon Marchegiani; Taylor Davis; Federico Tessadori; Gijs van Haaften; Francesco Brancati; Alexander Hoischen; Haigen Huang; Elise Valkanas; Barbara Pusey; Denny Schanze; Hanka Venselaar; Anneke T Vulto-van Silfhout; Lynne A Wolfe; Cynthia J Tifft; Patricia M Zerfas; Giovanna Zambruno; Ariana Kariminejad; Farahnaz Sabbagh-Kermani; Janice Lee; Maria G Tsokos; Chyi-Chia R Lee; Victor Ferraz; Eduarda Morgana da Silva; Cathy A Stevens; Nathalie Roche; Oliver Bartsch; Peter Farndon; Eva Bermejo-Sanchez; Brian P Brooks; Valerie Maduro; Bruno Dallapiccola; Feliciano J Ramos; Hon-Yin Brian Chung; Cédric Le Caignec; Fabiana Martins; Witold K Jacyk; Laura Mazzanti; Han G Brunner; Jeroen Bakkers; Shuo Lin; May Christine V Malicdan; Cornelius F Boerkoel; William A Gahl; Bert B A de Vries; Mieke M van Haelst; Martin Zenker; Thomas C Markello
Journal:  Am J Hum Genet       Date:  2015-06-25       Impact factor: 11.025

6.  Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).

Authors:  Tyler Mark Pierson; Thomas Markello; John Accardi; Lynne Wolfe; David Adams; Murat Sincan; Noor M Tarazi; Karin Fuentes Fajardo; Praveen F Cherukuri; Ilda Bajraktari; Katy G Meilleur; Sandra Donkervoort; Mina Jain; Ying Hu; Tanya J Lehky; Pedro Cruz; James C Mullikin; Carsten Bonnemann; William A Gahl; Cornelius F Boerkoel; Cynthia J Tifft
Journal:  Neuromuscul Disord       Date:  2013-03-01       Impact factor: 4.296

7.  Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.

Authors:  Orit Topaz; Daniel L Shurman; Reuven Bergman; Margarita Indelman; Paulina Ratajczak; Mordechai Mizrachi; Ziad Khamaysi; Doron Behar; Dan Petronius; Vered Friedman; Israel Zelikovic; Sharon Raimer; Arieh Metzker; Gabriele Richard; Eli Sprecher
Journal:  Nat Genet       Date:  2004-05-09       Impact factor: 38.330

8.  Chronic myopathy due to immunoglobulin light chain amyloidosis.

Authors:  Irini Manoli; Justin Y Kwan; Qian Wang; Elisabeth J Rushing; Maria Tsokos; Andrew E Arai; Warner M Burch; Angela Dispenzieri; Alexandra C McPherron; William A Gahl
Journal:  Mol Genet Metab       Date:  2013-02-04       Impact factor: 4.797

9.  Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.

Authors:  Jessica S Albert; Nisan Bhattacharyya; Lynne A Wolfe; William P Bone; Valerie Maduro; John Accardi; David R Adams; Charles E Schwartz; Joy Norris; Tim Wood; Rachel I Gafni; Michael T Collins; Laura L Tosi; Thomas C Markello; William A Gahl; Cornelius F Boerkoel
Journal:  Orphanet J Rare Dis       Date:  2015-03-07       Impact factor: 4.123

10.  Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.

Authors:  William P Bone; Nicole L Washington; Orion J Buske; David R Adams; Joie Davis; David Draper; Elise D Flynn; Marta Girdea; Rena Godfrey; Gretchen Golas; Catherine Groden; Julius Jacobsen; Sebastian Köhler; Elizabeth M J Lee; Amanda E Links; Thomas C Markello; Christopher J Mungall; Michele Nehrebecky; Peter N Robinson; Murat Sincan; Ariane G Soldatos; Cynthia J Tifft; Camilo Toro; Heather Trang; Elise Valkanas; Nicole Vasilevsky; Colleen Wahl; Lynne A Wolfe; Cornelius F Boerkoel; Michael Brudno; Melissa A Haendel; William A Gahl; Damian Smedley
Journal:  Genet Med       Date:  2015-11-12       Impact factor: 8.822

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  74 in total

1.  Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental Delay.

Authors:  Marie Morimoto; Helen Waller-Evans; Zineb Ammous; Xiaofei Song; Kevin A Strauss; Davut Pehlivan; Claudia Gonzaga-Jauregui; Erik G Puffenberger; Charles R Holst; Ender Karaca; Karlla W Brigatti; Emily Maguire; Zeynep H Coban-Akdemir; Akiko Amagata; C Christopher Lau; Xenia Chepa-Lotrea; Ellen Macnamara; Tulay Tos; Sedat Isikay; Michele Nehrebecky; John D Overton; Matthew Klein; Thomas C Markello; Jennifer E Posey; David R Adams; Emyr Lloyd-Evans; James R Lupski; William A Gahl; May Christine V Malicdan
Journal:  Am J Hum Genet       Date:  2018-10-25       Impact factor: 11.025

2.  Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B.

Authors:  Carlos R Ferreira; Dong Chen; Shirley M Abraham; David R Adams; Karen L Simon; May C Malicdan; Thomas C Markello; Meral Gunay-Aygun; William A Gahl
Journal:  Mol Genet Metab       Date:  2016-12-18       Impact factor: 4.797

3.  The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease.

Authors:  Rachel B Ramoni; John J Mulvihill; David R Adams; Patrick Allard; Euan A Ashley; Jonathan A Bernstein; William A Gahl; Rizwan Hamid; Joseph Loscalzo; Alexa T McCray; Vandana Shashi; Cynthia J Tifft; Anastasia L Wise
Journal:  Am J Hum Genet       Date:  2017-02-02       Impact factor: 11.025

4.  PARP1 inhibition alleviates injury in ARH3-deficient mice and human cells.

Authors:  Masato Mashimo; Xiangning Bu; Kazumasa Aoyama; Jiro Kato; Hiroko Ishiwata-Endo; Linda A Stevens; Atsushi Kasamatsu; Lynne A Wolfe; Camilo Toro; David Adams; Thomas Markello; William A Gahl; Joel Moss
Journal:  JCI Insight       Date:  2019-02-21

5.  MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

Authors:  Julia Wang; Rami Al-Ouran; Yanhui Hu; Seon-Young Kim; Ying-Wooi Wan; Michael F Wangler; Shinya Yamamoto; Hsiao-Tuan Chao; Aram Comjean; Stephanie E Mohr; Norbert Perrimon; Zhandong Liu; Hugo J Bellen
Journal:  Am J Hum Genet       Date:  2017-05-11       Impact factor: 11.025

6.  Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification.

Authors:  Elena-Raluca Nicoli; Mary R Weston; Mary Hackbarth; Alissa Becerril; Austin Larson; Wadih M Zein; Peter R Baker; John Douglas Burke; Heidi Dorward; Mariska Davids; Yan Huang; David R Adams; Patricia M Zerfas; Dong Chen; Thomas C Markello; Camilo Toro; Tim Wood; Gene Elliott; Mylinh Vu; Wei Zheng; Lisa J Garrett; Cynthia J Tifft; William A Gahl; Debra L Day-Salvatore; Joseph A Mindell; May Christine V Malicdan
Journal:  Am J Hum Genet       Date:  2019-05-30       Impact factor: 11.025

7.  Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.

Authors:  Teri A Manolio; Douglas M Fowler; Lea M Starita; Melissa A Haendel; Daniel G MacArthur; Leslie G Biesecker; Elizabeth Worthey; Rex L Chisholm; Eric D Green; Howard J Jacob; Howard L McLeod; Dan Roden; Laura Lyman Rodriguez; Marc S Williams; Gregory M Cooper; Nancy J Cox; Gail E Herman; Stephen Kingsmore; Cecilia Lo; Cathleen Lutz; Calum A MacRae; Robert L Nussbaum; Jose M Ordovas; Erin M Ramos; Peter N Robinson; Wendy S Rubinstein; Christine Seidman; Barbara E Stranger; Haoyi Wang; Monte Westerfield; Carol Bult
Journal:  Cell       Date:  2017-03-23       Impact factor: 41.582

8.  Clinical Genetic Screening in Adult Patients with Kidney Disease.

Authors:  Enrico Cocchi; Jordan Gabriela Nestor; Ali G Gharavi
Journal:  Clin J Am Soc Nephrol       Date:  2020-07-09       Impact factor: 8.237

9.  Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees.

Authors:  Stephanie A Zlatic; Alysia Vrailas-Mortimer; Avanti Gokhale; Lucas J Carey; Elizabeth Scott; Reid Burch; Morgan M McCall; Samantha Rudin-Rush; John Bowen Davis; Cortnie Hartwig; Erica Werner; Lian Li; Michael Petris; Victor Faundez
Journal:  Cell Syst       Date:  2018-01-31       Impact factor: 10.304

10.  Collaborative science unites researchers and a novel spastic ataxia gene.

Authors:  Brent L Fogel
Journal:  Ann Neurol       Date:  2018-06       Impact factor: 10.422

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