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PubPharm (49)
1
Advancing Precision Oncology in Hereditary Paraganglioma-Pheochromocytoma Syndromes : Integrated Interpretation and Data Sharing of the Germline and Tumor Genomes
enthalten in:
Cancers
| 2024
von
Rana, H.
|
Koeller, D.
|
Walker, M.
| +13
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2
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome : a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer
enthalten in:
Familial cancer
| 2023
von
Hodan, R.
|
Rodgers-Fouche, L.
|
Chittenden, A.
| +14
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3
Clinical factors associated with skin neoplasms in individuals with Lynch syndrome in a longitudinal observational cohort
enthalten in:
Journal of the American Academy of Dermatology
| 2023
von
Zhong, C.
|
Horiguchi, M.
|
Uno, H.
| +6
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4
Development and evaluation of INT2GRATE : a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome
enthalten in:
Frontiers in oncology
| 2023
von
Isidro, R.
|
Chittenden, A.
|
Walker, M.
| +13
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5
Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment
enthalten in:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
| 2022
von
Yurgelun, M.
|
Uno, H.
|
Furniss, C.
| +7
CommentIn: J Clin Oncol. 2022 Dec 10;40(35):4040-4043. - PMID 36166722
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6
Germline Testing for Individuals with Pancreatic Adenocarcinoma and Novel Genetic Risk Factors
enthalten in:
Hematology/oncology clinics of North America
| 2022
von
Chittenden, A.
|
Haraldsdottir, S.
|
Chen, E.
| +1
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7
Identification and Management of Pathogenic Variants in BRCA1, BRCA2, and PALB2 in a Tumor-Only Genomic Testing Program
enthalten in:
Clinical cancer research : an official journal of the American Association for Cancer Research
| 2022
von
Bychkovsky, B.
|
Li, T.
|
Sotelo, J.
| +20
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8
Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients
enthalten in:
Cancers
| 2022
von
Espinel, W.
|
Champine, M.
|
Hampel, H.
| +25
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9
An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes
enthalten in:
Frontiers in oncology
| 2022
von
Schwartz, A.
|
Manning, D.
|
Koeller, D.
| +12
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10
An optimized protocol for evaluating pathogenicity of VHL germline variants in patients suspected with von Hippel-Lindau syndrome : Using somatic genome to inform the role of germline variants
enthalten in:
MethodsX
| 2022
von
Koeller, D.
|
Manning, D.
|
Schwartz, A.
| +7
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49
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Familial cancer
6
Hereditary cancer in clinical practice
5
Journal of genetic counseling
2
Cancers
2
Frontiers in oncology
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Gastroenterology
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Hematology/oncology clinics of North America
1
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1
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1
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Thema
27
Journal Article
11
Research Support, N.I.H., Extramural
9
Research Support, Non-U.S. Gov't
6
Lynch syndrome
4
Ancestry
4
EC 3.6.1.3
4
Founder mutation testing strategy
4
Genetic testing
4
Lynch Syndrome
4
Polyposis in Ashkenazim
4
Review
3
-associated polyposis
3
Adaptor Proteins, Signal Transducing
3
Case Reports
3
Family
3
Genetic counseling
3
MLH1 protein, human
3
MutL Protein Homolog 1
3
Nuclear Proteins
3
Preimplantation genetic diagnosis
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Erscheinungszeitraum
17
2020-
24
2010-2019
8
2000-2009
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Englisch
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