Vanderbilt Center for Undiagnosed Diseases (VCUD)
Vanderbilt Center for Undiagnosed Diseases (VCUD)
批准号:
10677087
负责人:
JOY D COGAN
金额:
$75.03万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
已结题
起止时间:
2022-09-21 至 2023-04-30
关键词:
BioinformaticsCaregiversCaringClinicalClinical DataClinical ResearchClinical and Translational Science AwardsCollaborationsCounselingDNA DatabasesDataDatabasesDiagnosisDiagnostic ProcedureDiagnostic testsDifferential DiagnosisDiseaseEnsureFundingGenesGoalsHealthHealthcareHumanIndividualInsurance CarriersInternistLeadMedical GeneticsModelingNeurologistPatient CarePatientsPersonsPhasePhysiciansPopulationRecommendationResearchResearch PersonnelResourcesScientistSigns and SymptomsSpecialistStructureTest ResultTestingTimeTrainingTranslational ResearchUnited States Department of Veterans AffairsUnited States National Institutes of HealthUntranslated RNAVariantclinical research sitecohortexhaustimprovednext generationnext generation sequencingpatient orientedpediatricianprecision medicinestructural biology
中文摘要
项目总结
英文摘要
PROJECT SUMMARY
Undiagnosed Diseases (UD) are constellations of significant signs, symptoms and/or test results that are seen
by specialists over time without discovery of their cause(s), and for which diagnostic procedures and tests have
been exhausted. The goal of the Undiagnosed Disease Network (UDN) is to diagnose UDs and bring answers
that give afflicted individuals hope and ways to improve their health. Our Vanderbilt UDN Clinical Site (VCUD)
is an ideal milieu of excellent patient oriented care, and collaborative research. We formed the VCUD by
combining unique Vanderbilt resources with UDN resources to diagnose difficult UDs. Vanderbilt resources
include: 1) a productive Clinical and Translational Science Award that hosts a large Clinical Research Center
(CRC) that has grown, evolved, and developed an outstanding cohort of clinicians and physician scientists, 2)
a strong, dedicated group of Pediatricians, Internists, Neurologists and Geneticists, 3) bioinformatics experts,
4) the BioVU DNA databank and experts, 5) structural biology investigators, 6) our EMR and REDCap
database, and 7) a strong focus on educating and training the next generation who will help sustain the UDN
over the long-term. We have combined our VCUD team (physicians, bioinformatics experts, research
scientists, Study Coordinator, NPs, GCs), with UDN resources to diagnose UD patients by the following: A)
gathering and analyzing clinical data to form differential diagnoses (clinical hypotheses), B) analyzing next
generation sequencing and other test data to form testable gene hypotheses, C) utilizing unique VUMC
resources including BioVU, PrediXcan, and Structural Biology to prioritize candidate variants (CV), D)
determining the functional effects of non-coding CV, E) testing and merging our clinical and genetic
hypotheses to identify concordant disorders and CV that cause the patients’ UD, and F) using VCUD Studios
to discover new diseases and promote translational research to determine mechanisms and lead to
treatments. We hypothesize that we can use VCUD teams to merge patient care with translational research by
synergistically combining them with distinct VUMC resources to more efficiently diagnose and treat UD
patients. Our VCUD structure will provide the workflow, throughput, and passion needed to test our hypotheses
and diagnose and provide treatment recommendations. We will enhance all these activities in the Phase II
(UO1) expansion through collaborations with the UDN, the Veteran’s Administration, Precision Medicine
Projects and health care insurers, to produce an evolving and more sustainable model.
期刊论文(34)
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DOI:
10.1038/s41436-020-00984-z
发表时间:
2021-03
期刊:
Genetics in medicine : official journal of the American College of Medical Genetics
影响因子:
--
作者:
[Schoch K, Esteves C, Bican A, Spillmann R, Cope H, McConkie-Rosell A, Walley N, Fernandez L, Kohler JN, Bonner D, Reuter C, Stong N, Mulvihill JJ, Novacic D, Wolfe L, Abdelbaki A, Toro C, Tifft C, Malicdan M, Gahl W, Liu P, Newman J, Goldstein DB, Hom J, Sampson J, Wheeler MT, Undiagnosed Diseases Network, Cogan J, Bernstein JA, Adams DR, McCray AT, Shashi V]
通讯作者:
Shashi V
DOI:
10.1542/peds.2022-057010
发表时间:
2022-05-01
期刊:
Pediatrics
影响因子:
8
作者:
[Bull, Marilyn J, Trotter, Tracy, Spire, Paul]
通讯作者:
Spire, Paul
DOI:
10.1002/ajmg.a.61558
发表时间:
2020-06
期刊:
American journal of medical genetics. Part A
影响因子:
--
作者:
[Burdick KJ, Cogan JD, Rives LC, Robertson AK, Koziura ME, Brokamp E, Duncan L, Hannig V, Pfotenhauer J, Vanzo R, Paul MS, Bican A, Morgan T, Duis J, Newman JH, Hamid R, Phillips JA 3rd, Undiagnosed Diseases Network]
通讯作者:
Undiagnosed Diseases Network
Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation.
遗传咨询师在未确诊疾病网络研究中的作用:临床护理、合作和管理。
DOI:
10.1002/jgc4.1493
发表时间:
2022
期刊:
Journal of genetic counseling
影响因子:
1.9
作者:
[Kohler,JenneferN, Kelley,EmilyG, Boyd,BrennaM, Sillari,CatherineH, Marwaha,Shruti, UndiagnosedDiseasesNetwork, Wheeler,MatthewT]
通讯作者:
Wheeler,MatthewT
DOI:
10.1164/rccm.201610-2111ed
发表时间:
2017
期刊:
American journal of respiratory and critical care medicine
影响因子:
24.7
作者:
[Hamid,Rizwan, Yan,Ling]
通讯作者:
Yan,Ling
共 16 条
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:10600283
-
项目类别:
-
资助金额:$30.2万
-
财政年份:2022
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD) - Biorepository
-
批准号:10600407
-
项目类别:
-
资助金额:$6.0万
-
财政年份:2022
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:10405736
-
项目类别:
-
资助金额:$10.45万
-
财政年份:2014
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:9788515
-
项目类别:
-
资助金额:$150.0万
-
财政年份:2014
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:9930322
-
项目类别:
-
资助金额:$14.24万
-
财政年份:2014
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:10871541
-
项目类别:
-
资助金额:$33.19万
-
财政年份:2014
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:10200110
-
项目类别:
-
资助金额:$110.0万
-
财政年份:2014
-
负责人:JOY D COGAN
-
依托单位:
Vanderbilt Center for Undiagnosed Diseases (VCUD)
-
批准号:10696591
-
项目类别:
-
资助金额:$68.13万
-
财政年份:2014
-
负责人:JOY D COGAN
-
依托单位:
BASIS OF COMBINED PITUITARY HORMONE DEFICIENCY
-
批准号:2905969
-
项目类别:
-
资助金额:$18.88万
-
财政年份:1997
-
负责人:JOY D COGAN
-
依托单位:
BASIS OF COMBINED PITUITARY HORMONE DEFICIENCY
-
批准号:2734233
-
项目类别:
-
资助金额:$18.68万
-
财政年份:1997
-
负责人:JOY D COGAN
-
依托单位:
BASIS OF COMBINED PITUITARY HORMONE DEFICIENCY
-
批准号:2017828
-
项目类别:
-
资助金额:$18.47万
-
财政年份:1997
-
负责人:JOY D COGAN
-
依托单位:
海外基金