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

Ming Tan; Klaus Brusgaard; Anne-Marie Gerdes; Martin Jakob Larsen; Michael Bau Mortensen; Sönke Detlefsen; Ove B Schaffalitzky de Muckadell; Maiken Thyregod Joergensen

doi:10.1111/ahg.12464

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

^*Corresponding author for this work

Rigshospitalet

Research output: Contribution to journal › Journal article › Research › peer-review

173 Downloads (Pure)

Original language	English
Journal	Annals of Human Genetics
Volume	86
Issue number	4
Pages (from-to)	195-206
ISSN	0003-4800
DOIs	https://doi.org/10.1111/ahg.12464
Publication status	Published - Jul 2022

Keywords

familial pancreatic cancers
pancreatic ductal adenocarcinoma
protein truncating variants
rare variants
whole genome sequencing
Genetic Predisposition to Disease
Carcinoma
Humans
Pancreatic Neoplasms/genetics
Whole Genome Sequencing

Documents & Links

10.1111/ahg.12464Licence: CC BY-NC-ND

Open Access VersionFinal published version, 418 KBLicence: CC BY-NC-ND

SDU Link

Check access to the material in SDU Library's search engine

Whole genome sequencing analysis of familial pancreatic cancer in a Danish cohort
Tan, M., 15. Mar 2022, Syddansk Universitet. Det Sundhedsvidenskabelige Fakultet. 140 p.
Research output: Thesis › Ph.D. thesis

Open Access
File
28 Downloads (Pure)

Cite this

@article{88f99f7b279e4952b26faacdb11dc3ae,

title = "Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients",

keywords = "familial pancreatic cancers, pancreatic ductal adenocarcinoma, protein truncating variants, rare variants, whole genome sequencing, Genetic Predisposition to Disease, Carcinoma, Humans, Pancreatic Neoplasms/genetics, Whole Genome Sequencing",

author = "Ming Tan and Klaus Brusgaard and Anne-Marie Gerdes and Larsen, \{Martin Jakob\} and Mortensen, \{Michael Bau\} and S{\"o}nke Detlefsen and \{de Muckadell\}, \{Ove B Schaffalitzky\} and Joergensen, \{Maiken Thyregod\}",

year = "2022",

month = jul,

doi = "10.1111/ahg.12464",

language = "English",

volume = "86",

pages = "195--206",

journal = "Annals of Human Genetics",

issn = "0003-4800",

publisher = "Wiley",

number = "4",

}

TY - JOUR

T1 - Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients

AU - Tan, Ming

AU - Brusgaard, Klaus

AU - Gerdes, Anne-Marie

AU - Larsen, Martin Jakob

AU - Mortensen, Michael Bau

AU - Detlefsen, Sönke

AU - de Muckadell, Ove B Schaffalitzky

AU - Joergensen, Maiken Thyregod

PY - 2022/7

Y1 - 2022/7

KW - familial pancreatic cancers

KW - pancreatic ductal adenocarcinoma

KW - protein truncating variants

KW - rare variants

KW - whole genome sequencing

KW - Genetic Predisposition to Disease

KW - Carcinoma

KW - Humans

KW - Pancreatic Neoplasms/genetics

KW - Whole Genome Sequencing

U2 - 10.1111/ahg.12464

DO - 10.1111/ahg.12464

M3 - Journal article

C2 - 35312039

SN - 0003-4800

VL - 86

SP - 195

EP - 206

JO - Annals of Human Genetics

JF - Annals of Human Genetics

IS - 4

ER -

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

Keywords

Documents & Links

SDU Link

Related research output

Whole genome sequencing analysis of familial pancreatic cancer in a Danish cohort

Cite this