Integrated Whole-Genome Analysis of Hematologic Disorders
NCT ID: NCT01108159
Last Updated: 2018-05-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
35 participants
OBSERVATIONAL
2009-09-30
2013-08-02
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Blood Draw
Skin Biopsy
Eligibility Criteria
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Inclusion Criteria
2. Patient meets the clinical and/or pathologic criteria for the hematologic disorder being examined.
3. Patient is willing to provide a skin biopsy and five 10 mL tubes of peripheral blood.
Exclusion Criteria
2. Patient is not willing to provide a skin biopsy and five 10 mL tubes of peripheral blood.
18 Years
ALL
No
Sponsors
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Stanford University
OTHER
Responsible Party
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Jason D. Merker
Assistant Professor of Pathology
Principal Investigators
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James L Zehnder
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Locations
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Stanford University School of Medicine
Stanford, California, United States
Countries
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References
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Merker JD, Roskin KM, Ng D, Pan C, Fisk DG, King JJ, Hoh R, Stadler M, Okumoto LM, Abidi P, Hewitt R, Jones CD, Gojenola L, Clark MJ, Zhang B, Cherry AM, George TI, Snyder M, Boyd SD, Zehnder JL, Fire AZ, Gotlib J. Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes. Haematologica. 2013 Nov;98(11):1689-96. doi: 10.3324/haematol.2013.092379. Epub 2013 Jul 19.
Other Identifiers
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1081737-100-DHAAT
Identifier Type: -
Identifier Source: secondary_id
SU-09092009-3820
Identifier Type: OTHER
Identifier Source: secondary_id
16329
Identifier Type: OTHER
Identifier Source: secondary_id
HEM0013
Identifier Type: -
Identifier Source: org_study_id
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