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Huma Q Rana

Showing results (31-40 of 75) with videos related to

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Cancer|April 2, 2019
Prevalence of germline variants in inflammatory breast cancerHuma Q Rana, Rosalba Sacca, Christine Drogan, et al.
Gynecologic Oncology|November 24, 2020
Embedding a genetic counselor into oncology clinics improves testing rates and timeliness for women with ovarian cancerHuma Q Rana, Lindsay Kipnis, Kristin Hehir, et al.
Methodsx|July 1, 2022
An optimized protocol for evaluating pathogenicity of <i>VHL</i> germline variants in patients suspected with von Hippel-Lindau syndrome: Using somatic genome to inform the role of germline variantsDiane R Koeller, Danielle K Manning, Alison Schwartz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 21, 2019
Genotype-phenotype associations among panel-based TP53+ subjectsHuma Q Rana, Jacob Clifford, Lily Hoang, et al.
Cancer Genetics|February 27, 2022
Vulvar Melanoma in association with germline MITF p.E318K variantDiane R Koeller, Alison Schwartz, Mia S DeSimone, et al.
European Journal of Medical Genetics|October 10, 2021
Pathogenicity of VHL variants in families with non-syndromic von Hippel-Lindau phenotypes: An integrated evaluation of germline and somatic genomic resultsHuma Q Rana, Diane R Koeller, Alison Schwartz, et al.
Genetics in Medicine Open|December 13, 2024
Cancer burden in individuals with single versus double pathogenic variants in cancer susceptibility genesNihat B Agaoglu, Brittany L Bychkovsky, Carolyn Horton, et al.
Psycho-Oncology|January 23, 2026
Maternal Communication of BRCA Risk to Adolescent and Young Adult Children: Implications for Supportive Care InterventionMuriel R Statman, Marcelo M Sleiman, Beth N Peshkin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 13, 2016
Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics StudyStacy W Gray, Sarah E Gollust, Deanna Alexis Carere, et al.
JAMA Oncology|September 22, 2022
Differences in Cancer Phenotypes Among Frequent CHEK2 Variants and Implications for Clinical Care-Checking CHEK2Brittany L Bychkovsky, Nihat B Agaoglu, Carolyn Horton, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Cancer|April 2, 2019
Prevalence of germline variants in inflammatory breast cancerHuma Q Rana, Rosalba Sacca, Christine Drogan, et al.
Gynecologic Oncology|November 24, 2020
Embedding a genetic counselor into oncology clinics improves testing rates and timeliness for women with ovarian cancerHuma Q Rana, Lindsay Kipnis, Kristin Hehir, et al.
Methodsx|July 1, 2022
An optimized protocol for evaluating pathogenicity of <i>VHL</i> germline variants in patients suspected with von Hippel-Lindau syndrome: Using somatic genome to inform the role of germline variantsDiane R Koeller, Danielle K Manning, Alison Schwartz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 21, 2019
Genotype-phenotype associations among panel-based TP53+ subjectsHuma Q Rana, Jacob Clifford, Lily Hoang, et al.
Cancer Genetics|February 27, 2022
Vulvar Melanoma in association with germline MITF p.E318K variantDiane R Koeller, Alison Schwartz, Mia S DeSimone, et al.
European Journal of Medical Genetics|October 10, 2021
Pathogenicity of VHL variants in families with non-syndromic von Hippel-Lindau phenotypes: An integrated evaluation of germline and somatic genomic resultsHuma Q Rana, Diane R Koeller, Alison Schwartz, et al.
Genetics in Medicine Open|December 13, 2024
Cancer burden in individuals with single versus double pathogenic variants in cancer susceptibility genesNihat B Agaoglu, Brittany L Bychkovsky, Carolyn Horton, et al.
Psycho-Oncology|January 23, 2026
Maternal Communication of BRCA Risk to Adolescent and Young Adult Children: Implications for Supportive Care InterventionMuriel R Statman, Marcelo M Sleiman, Beth N Peshkin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 13, 2016
Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics StudyStacy W Gray, Sarah E Gollust, Deanna Alexis Carere, et al.
JAMA Oncology|September 22, 2022
Differences in Cancer Phenotypes Among Frequent CHEK2 Variants and Implications for Clinical Care-Checking CHEK2Brittany L Bychkovsky, Nihat B Agaoglu, Carolyn Horton, et al.
Pageof 8