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Author Details
Full Name
Peter V Grauman
Affiliation
ORCID
Career Start Year
2014
Papers
11
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
31036917
Sequencing as a first-line methodology for cystic fibrosis carrier screening.
Genetics in Medicine
2019
31089271
Correction: Sequencing as a first-line methodology for cystic fibrosis carrier screening.
Genetics in Medicine
2019
29760218
Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification.
Clin Chem
2018
30268105
Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene.
BMC Med Genet
2018
28243543
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment.
PeerJ
2017
29018079
<i>SETD2</i> alterations impair DNA damage recognition and lead to resistance to chemotherapy in leukemia.
Blood
2017
28177873
Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation.
New England Journal of Medicine
2017
25550361
Acute myeloid leukemia ontogeny is defined by distinct somatic mutations.
Blood
2015
24662245
Mutations in epigenetic regulators including SETD2 are gained during relapse in paediatric acute lymphoblastic leukaemia.
Nat Commun
2014
24292625
Lenalidomide causes selective degradation of IKZF1 and IKZF3 in multiple myeloma cells.
Science
2014
25426837
Age-related clonal hematopoiesis associated with adverse outcomes.
N Engl J Med
2014
1 - 11 of 11
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