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Wiszniewska, Joanna
98
results:
Search for persons
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Online (98)
Mediatypes
Articles (Online) (40)
Bookchapter (Online) (1)
OpenAccess-fulltext (57)
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1
Performance Evaluation of a Novel Artificial Intelligence–A..:
Bagg, Adam
;
Raess, Philipp W.
;
Rund, Deborah
...
Modern Pathology. 37 (2024) 9 - p. 100542 , 2024
Link:
https://doi.org/10.1016/..
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2
Pediatric autoimmune myelofibrosis: Experience from a large..:
Kim, Taylor Olmsted
;
Curry, Choladda V.
;
Wiszniewska, Joanna
...
Pediatric Blood & Cancer. 70 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1002/..
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3
Histopathological and molecular findings in a patient with ..:
Xie, Wei
;
Fan, Guang
;
Wiszniewska, Joanna
..
Human Pathology Reports. 29 (2022) - p. 300670 , 2022
Link:
https://doi.org/10.1016/..
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4
An Organismal CNV Mutator Phenotype Restricted to Early Hum..:
Liu, Pengfei
;
Yuan, Bo
;
Carvalho, Claudia M.B.
...
Cell. 168 (2017) 5 - p. 830-842.e7 , 2017
Link:
https://doi.org/10.1016/..
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5
Donor Cell-Derived Myelodysplastic Syndrome in Pediatric He..:
Wiszniewska, Joanna
;
Leung, Kathryn
;
Sasa, Ghadir
..
American Journal of Clinical Pathology. 142 (2014) suppl_1 - p. A132-A132 , 2014
Link:
https://doi.org/10.1093/..
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6
Multiple de novo copy number variations in two subjects wit..:
Liu, Pengfei
;
Walter, Klaudia
;
Writzl, Karin
...
BMC Proceedings. 6 (2012) S6 - p. , 2012
Link:
https://doi.org/10.1186/..
?
7
WDR62 missense mutation in a consanguineous family with pri..:
Bacino, Carlos A.
;
Arriola, Luis A.
;
Wiszniewska, Joanna
.
American Journal of Medical Genetics Part A. 158A (2012) 3 - p. 622-625 , 2012
Link:
https://doi.org/10.1002/..
?
8
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are ..:
Celestino-Soper, Patrícia BS
;
Skinner, Cindy
;
Schroer, Richard
...
Molecular Cytogenetics. 5 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
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9
De novo interstitial duplication of 15q11.2–q13.1 with comp..:
Burrage, Lindsay C.
;
Person, Richard E.
;
Flores, Angela
...
American Journal of Medical Genetics Part A. 158A (2012) 10 - p. 2557-2563 , 2012
Link:
https://doi.org/10.1002/..
?
10
Observation and prediction of recurrent human translocation..:
Ou, Zhishuo
;
Stankiewicz, Paweł
;
Xia, Zhilian
...
Genome Research. 21 (2011) 1 - p. 33-46 , 2011
Link:
https://doi.org/10.1101/..
?
11
Detection of uniparental isodisomy in autosomal recessive m..:
Douglas, Ganka V
;
Wiszniewska, Joanna
;
Lipson, Mark H
...
Journal of Human Genetics. 56 (2011) 12 - p. 834-839 , 2011
Link:
https://doi.org/10.1038/..
?
12
Chromosome Catastrophes Involve Replication Mechanisms Gene..:
Liu, Pengfei
;
Erez, Ayelet
;
Nagamani, Sandesh C. Sreenath
...
Cell. 146 (2011) 6 - p. 889-903 , 2011
Link:
https://doi.org/10.1016/..
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13
Copy number gain at Xp22.31 includes complex duplication re..:
Liu, Pengfei
;
Erez, Ayelet
;
Sreenath Nagamani, Sandesh C.
...
Human Molecular Genetics. 20 (2011) 10 - p. 1975-1988 , 2011
Link:
https://doi.org/10.1093/..
?
14
Copy Number and SNP Arrays in Clinical Diagnostics:
Schaaf, Christian P.
;
Wiszniewska, Joanna
;
Beaudet, Arthur L.
Annual Review of Genomics and Human Genetics. 12 (2011) 1 - p. 25-51 , 2011
Link:
https://doi.org/10.1146/..
?
15
Deoxyguanosine kinase deficiency presenting as neonatal hem..:
Hanchard, Neil A.
;
Shchelochkov, Oleg A.
;
Roy, Angshumoy
...
Molecular Genetics and Metabolism. 103 (2011) 3 - p. 262-267 , 2011
Link:
https://doi.org/10.1016/..
1-15