Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients-Reference-Cited by-同舟云学术

Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients

Published:2022-03-21 Issue:4 Volume:86 Page:195-206
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Tan Ming¹²³,Brusgaard Klaus¹⁴,Gerdes Anne‐Marie⁵,Larsen Martin Jakob¹⁴,Mortensen Michael Bau¹³⁶,Detlefsen Sönke¹³⁷,de Muckadell Ove B. Schaffalitzky¹²³,Joergensen Maiken Thyregod¹²³

Affiliation:

1. Department of Clinical Research University of Southern Denmark Odense Denmark

2. Department of Medical Gastroenterology Odense University Hospital Odense Denmark

3. Odense Pancreas Center (OPAC) Odense University Hospital Odense Denmark

4. Department of Clinical Genetics Odense University Hospital Odense Denmark

5. Department of Clinical Genetics Rigshospitalet Copenhagen Denmark

6. Department of Surgery Odense University Hospital Odense Denmark

7. Department of Pathology Odense University Hospital Odense Denmark

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12464

Reference45 articles.

1. Identification of germline genomic copy number variation in familial pancreatic cancer

2. POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance

3. Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

4. Prevalence of germ-line mutations in cancer genes among pancreatic cancer patients with a positive family history

5. Familial Pancreatic Ductal Adenocarcinoma