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

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

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Originalsprog	Engelsk
Tidsskrift	Annals of Human Genetics
Vol/bind	86
Udgave nummer	4
Sider (fra-til)	195-206
ISSN	0003-4800
DOI	https://doi.org/10.1111/ahg.12464
Status	Udgivet - jul. 2022

Dokumenter og links

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

Open Access VersionForlagets udgivne version, 418 KBLicens: CC BY-NC-ND

1 Ph.d.-afhandling

Whole genome sequencing analysis of familial pancreatic cancer in a Danish cohort
Tan, M., 15. mar. 2022, Syddansk Universitet. Det Sundhedsvidenskabelige Fakultet. 140 s.
Publikation: Afhandling › Ph.d.-afhandling

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Citationsformater

@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

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

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