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Cancer Medicine
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February 15, 2025
Delivering Trio Germline Whole Genome Sequencing to Patients Newly Diagnosed With Childhood Cancer: Healthcare Professionals' Perspectives of the PREDICT Study
Jacqueline D Hunter, Kate Hetherington, Claire E Wakefield, et al.
The Journal of Organic Chemistry
|
April 28, 2009
Process research and development for a tetrazole-based growth hormone secretagogue (GHS) pharmaceutical development candidate
Akin H Davulcu, Douglas D McLeod, Jun Li, et al.
BMC Cancer
|
July 31, 2012
How should we discuss genetic testing with women newly diagnosed with breast cancer? Design and implementation of a randomized controlled trial of two models of delivering education about treatment-focused genetic testing to younger women newly diagnosed with breast cancer
Kaaren J Watts, Bettina Meiser, Gillian Mitchell, et al.
Journal of Community Genetics
|
April 3, 2023
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study
Laura Wedd, Margaret Gleeson, Bettina Meiser, et al.
European Journal of Human Genetics : EJHG
|
March 31, 2018
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history
Bettina Meiser, Veronica F Quinn, Gillian Mitchell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 30, 2016
Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial
Veronica F Quinn, Bettina Meiser, Judy Kirk, et al.
Translational Oncology
|
January 10, 2025
Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 16, 2024
Adenomas from individuals with pathogenic biallelic variants in the <i>MUTYH</i> and <i>NTHL1</i> genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Cancers
|
October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
Romy Walker, Khalid Mahmood, Julia Como, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
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Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Cancer Medicine
|
February 15, 2025
Delivering Trio Germline Whole Genome Sequencing to Patients Newly Diagnosed With Childhood Cancer: Healthcare Professionals' Perspectives of the PREDICT Study
Jacqueline D Hunter, Kate Hetherington, Claire E Wakefield, et al.
The Journal of Organic Chemistry
|
April 28, 2009
Process research and development for a tetrazole-based growth hormone secretagogue (GHS) pharmaceutical development candidate
Akin H Davulcu, Douglas D McLeod, Jun Li, et al.
BMC Cancer
|
July 31, 2012
How should we discuss genetic testing with women newly diagnosed with breast cancer? Design and implementation of a randomized controlled trial of two models of delivering education about treatment-focused genetic testing to younger women newly diagnosed with breast cancer
Kaaren J Watts, Bettina Meiser, Gillian Mitchell, et al.
Journal of Community Genetics
|
April 3, 2023
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study
Laura Wedd, Margaret Gleeson, Bettina Meiser, et al.
European Journal of Human Genetics : EJHG
|
March 31, 2018
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history
Bettina Meiser, Veronica F Quinn, Gillian Mitchell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 30, 2016
Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial
Veronica F Quinn, Bettina Meiser, Judy Kirk, et al.
Translational Oncology
|
January 10, 2025
Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 16, 2024
Adenomas from individuals with pathogenic biallelic variants in the <i>MUTYH</i> and <i>NTHL1</i> genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Cancers
|
October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
Romy Walker, Khalid Mahmood, Julia Como, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Page
of 5