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Nicole L. Hoppman‐Chaney
Observed names:
N Hoppman‐Chaney,
Nicole Hoppman-Chaney,
Nicole Hoppman‐Chaney,
Nicole L Hoppman-Chaney,
Nicole L. Hoppman-Chaney
Institution:
Mayo Clinic
Observed institution:
Mayo Clinic
OpenAlex ID:
A5047729488
Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype
2012
·
N Hoppman‐Chaney
, K Wain
, et al.
·
Clinical Genetics
·
128
Evaluation of Oligonucleotide Sequence Capture Arrays and Comparison of Next-Generation Sequencing Platforms for Use in Molecular Diagnostics
2010
·
Nicole Hoppman-Chaney
, Lisa M Peterson
, et al.
·
Clinical Chemistry
·
50
Expanding DNA diagnostic panel testing: is more better?
2011
·
Eric W Klee
, Nicole L Hoppman-Chaney
, et al.
·
Expert Review of Molecular Diagnostics
·
48
Partial hexasomy for the Prader–Willi–Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome
2010
·
Nicole L. Hoppman‐Chaney
, D. Brian Dawson
, et al.
·
American Journal of Medical Genetics Part A
·
43
In‐frame multi‐exon deletion of SMC1A in a severely affected female with Cornelia de Lange Syndrome
2011
·
Nicole Hoppman‐Chaney
, Jin Sung Jang
, et al.
·
American Journal of Medical Genetics Part A
·
25
Identification of a patient with 7q32 deletion–associated acute myeloid leukemia and an incidental t(8;14)
2010
·
Nicole L. Hoppman-Chaney
, Daniel Cherry
, et al.
·
Cancer Genetics and Cytogenetics
·
5
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Works count:
6
Citation count:
299
H-index:
5
I10-index:
5
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