Diane R. Koeller

发表

Transgender patients’ perspectives on their cancer genetic counseling experiences

Lathel Rolle, Kimberly Zayhowski, Diane R. Koeller, 2021, Journal of genetic counseling.

Trans‐counseling: A case series of transgender individuals at high risk for BRCA1 pathogenic variants

J. Garber, H. Rana, D. Morganstern, 2019, Journal of genetic counseling.

Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients

R. Nussbaum, S. Lincoln, J. Stopfer, 2022, Cancers.

Pathogenicity of VHL variants in families with non-syndromic von Hippel-Lindau phenotypes: An integrated evaluation of germline and somatic genomic results.

Danielle K. Manning, T. Choueiri, J. Garber, 2021, European journal of medical genetics.

An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes

Danielle K. Manning, J. Garber, H. Rana, 2022, Frontiers in Oncology.

Call for action: expanding global access to hereditary cancer genetic testing.

A. Taghian, F. Ademuyiwa, H. Rana, 2022, The Lancet. Oncology.

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

Danielle K. Manning, J. Garber, N. Lindeman, 2022, MethodsX.

Hereditary Lung Cancer Risk: Recent Discoveries and Implications for Genetic Counseling and Testing

G. Oxnard, Diane R. Koeller, Ruthia Chen, 2018, Current Genetic Medicine Reports.

Assessment of genomic alterations in non-syndromic von Hippel-Lindau: Insight from integrating somatic and germline next generation sequencing genomic data.

Danielle K. Manning, J. Garber, N. Lindeman, 2021, Data in brief.

Novel Pathogenic Germline Variant of the Adenomatous Polyposis Coli (APC) Gene, p.S2627Gfs*12 Identified in a Mild Phenotype of APC-Associated Polyposis: A Case Report

Danielle K. Manning, J. Garber, N. Lindeman, 2020, The American journal of case reports.

Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices

B. Yashar, Diane R. Koeller, Bailey Hulswit, 2022, Journal of genetic counseling.

Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study

Kimberly Zayhowski, Diane R. Koeller, Tala Berro, 2021, Journal of community genetics.

Vulvar Melanoma in association with germline MITF p.E318K variant.

J. Garber, N. Lindeman, H. Rana, 2022, Cancer genetics.

Utilization of Genetic Counseling after Direct-to-Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study

R. Green, J. Roberts, W. Uhlmann, 2017, Journal of Genetic Counseling.

OA 06.02 Final Report of the INHERIT EGFR Study - 33 Unrelated Kindreds Carrying Germline EGFR Mutations

J. Garber, G. Wiesner, G. Oxnard, 2017 .

Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives

R. Green, J. Roberts, W. Uhlmann, 2020, Journal of genetic counseling.

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

G. Idos, Jessica M. Long, Danielle B. McKenna, 2023, Familial Cancer.

Pretest Video Education Versus Genetic Counseling for Patients With Prostate Cancer: ProGen, A Multisite Randomized Controlled Trial

G. Sonpavde, E. Heath, H. Rana, 2023, JCO oncology practice.