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PubPharm (155)
1
Universal germline genetic testing in patients with hematologic malignancies using DNA isolated from nail clippings
enthalten in:
Haematologica
| 2024
von
Ceyhan-Birsoy, O.
|
Fiala, E.
|
Rana, S.
| +42
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2
Microsatellite Instability and Mismatch Repair Deficiency Define a Distinct Subset of Lung Cancers Characterized by Smoking Exposure, High Tumor Mutational Burden, and Recurrent Somatic MLH1 Inactivation
enthalten in:
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
| 2024
von
Yang, S.
|
Gedvilaite, E.
|
Ptashkin, R.
| +16
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3
Mainstreaming in parallel with ovarian cancer tumor testing to improve genetic testing uptake
enthalten in:
Gynecologic oncology
| 2024
von
Byrne, M.
|
Sia, T.
|
Fong, C.
| +21
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4
Cell-free DNA from nail clippings as source of normal control for genomic studies in hematologic malignancies
enthalten in:
Haematologica
| 2024
von
Krystel-Whittemore, M.
|
Petrova-Drus, K.
|
Ptashkin, R.
| +45
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5
Genomic ancestry in kidney cancer : Correlations with clinical and molecular features
enthalten in:
Cancer
| 2024
von
Kotecha, R.
|
Knezevic, A.
|
Arora, K.
| +14
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6
Nonlobular Invasive Breast Carcinomas with Biallelic Pathogenic CDH1 Somatic Alterations : A Histologic, Immunophenotypic, and Genomic Characterization
enthalten in:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
| 2024
von
Derakhshan, F.
|
Da Cruz Paula, A.
|
Selenica, P.
| +17
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7
Pathogenic germline variants in patients with endometrial cancer of diverse ancestry
enthalten in:
Cancer
| 2024
von
Liu, Y.
|
Gordhandas, S.
|
Arora, K.
| +28
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8
Pathogenic germline variants in non-BRCA1/2 homologous recombination genes in ovarian cancer : Analysis of tumor phenotype and survival
enthalten in:
Gynecologic oncology
| 2024
von
Kahn, R.
|
Selenica, P.
|
Boerner, T.
| +25
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9
Genomic ancestry in kidney cancer : Correlations with clinical and molecular features
enthalten in:
Cancer
| 2024
von
Kotecha, R.
|
Knezevic, A.
|
Arora, K.
| +14
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10
Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variants
enthalten in:
bioRxiv.org
| 2023
von
Huang, H.
|
Hu, C.
|
Na, J.
| +20
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