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PubPharm (83)
1
Increased prevalence of germline pathogenic CHEK2 variants in individuals with pituitary adenomas
enthalten in:
The Journal of clinical endocrinology and metabolism
| 2024
von
De Sousa, S.
|
McCormack, A.
|
Orsmond, A.
| +9
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2
Author Correction : Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death
enthalten in:
Nature medicine
| 2024
von
Byrne, A.
|
Arts, P.
|
Ha, T.
| +129
ErratumFor: Nat Med. 2023 Jan;29(1):180-189. - PMID 36658419
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3
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
enthalten in:
Blood advances
| 2023
von
Homan, C.
|
Drazer, M.
|
Yu, K.
| +63
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4
Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention
enthalten in:
Haematologica
| 2023
von
Shanmuganathan, N.
|
Wadham, C.
|
Shahrin, N.
| +21
CommentIn: Haematologica. 2023 Sep 01;108(9):2273-2274. - PMID 37078263
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5
Novel modes of MPL activation in triple-negative myeloproliferative neoplasms
enthalten in:
Pathology
| 2023
von
Samaraweera, S.
|
Geukens, T.
|
Casolari, D.
| +17
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6
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death
enthalten in:
Nature medicine
| 2023
von
Byrne, A.
|
Arts, P.
|
Ha, T.
| +129
CommentIn: Nat Med. 2023 Jan;29(1):41-42. - PMID 36670297
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7
Genomic instability drives tumorigenesis and metastasis and its implications for cancer therapy
enthalten in:
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
| 2023
von
Guo, S.
|
Zhu, X.
|
Huang, Z.
| +6
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8
Machine learning models-based on integration of next-generation sequencing testing and tumor cell sizes improve subtype classification of mature B-cell neoplasms
enthalten in:
Frontiers in oncology
| 2023
von
Mu, Y.
|
Chen, Y.
|
Meng, Y.
| +11
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9
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations
enthalten in:
Blood advances
| 2022
von
Drazer, M.
|
Homan, C.
|
Yu, K.
| +20
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10
RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia
enthalten in:
The Journal of molecular diagnostics : JMD
| 2022
von
Shanmuganathan, N.
|
Wadham, C.
|
Thomson, D.
| +17
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BMC endocrine disorders
6
Journal of molecular medicine
4
Blood
4
Bulletin of environmental contamination and tox...
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Endocrine pathology
4
Haematologica
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BMC medical genetics
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American journal of medical genetics. Part A
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Thema
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28
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7
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7
Whole exome sequencing
4
Copy number variation
4
Driver mutation
4
Letter
4
Loss of heterozygosity
4
N-containing groups
4
Pituitary adenoma
4
Polydopamine
4
Prolactinoma
4
Research Support, N.I.H., Extramural
4
Sorption
3
AKT
3
Aryl hydrocarbon receptor
3
Biomarkers, Tumor
3
Clock genes
3
Congenital neutropenia
3
Core Binding Factor Alpha 2 Subunit
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Erscheinungszeitraum
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2020-
39
2010-2019
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2000-2009
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