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Screening of HELQ in breast and ovarian cancer families

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-015-9838-4
Pelttari, Liisa M.; Kinnunen, Laura; Kiiski, Johanna I.; Khan, Sofia; Blomqvist, Carl; Aittomaki, Kr...
Familial cancer2016

Constitutional mosaicism for aBRCA2mutation as a cause of early-onset breast cancer

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-020-00186-1
Alhopuro, Pia; Vainionpää, Reetta; Anttonen, Anna-Kaisa; Aittomäki, Kristiina; Nevanlinna, Heli; Pöy...
Familial cancer2020

Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis

Referentgranskad
DOI
10.1007/s10689-014-9773-9
Koskenvuo, L.; Mustonen, H.; Renkonen-Sinisalo, L.; Jarvinen, H. J.; Lepistö, A.
Familial cancer2015

Hereditary leiomyomatosis and renal cell cancer (HLRCC):renal cancer risk, surveillance and treatment

Referentgranskad
DOI
10.1007/s10689-014-9735-2
Menko, Fred H.; Maher, Eamonn R.; Schmidt, Laura S.; Middelton, Lindsay A.; Aittomaki, Kristiina; To...
Familial cancer2014

Can our experience with surveillance for inherited pancreatic cancer help to identify early pancreatic cancer in the general population?

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-024-00363-6
Loehr, J. Matthias; Oehlund, Daniel; Soreskog, Emma; Andersson, Emil; Vujasinovic, Miroslav; Zethrae...
Familial cancer2024

Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer

Referentgranskad
DOI
10.1007/s10689-015-9778-z
Donner, Iikki; Kiviluoto, Tuula; Ristimaki, Ari; Aaltonen, Lauri A.; Vahteristo, Pia
Familial cancer2015

Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer

Referentgranskad
DOI
10.1007/s10689-012-9532-8
Saarinen, Silva; Vahteristo, Pia; Lehtonen, Rainer; Aittomäki, Kristiina; Launonen, Virpi; Kiviluoto...
Familial cancer2012

3 '-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity

Referentgranskad
DOI
10.1007/s10689-015-9804-1
Kondelin, Johanna; Tuupanen, Sari; Gylfe, Alexandra E.; Aavikko, Mervi; Renkonen-Sinisalo, Laura; JÃ...
Familial cancer2015

Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD)

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-020-00193-2
Seppälä, Toni T.; Dominguez-Valentin, Mev; Sampson, Julian R.; Møller, Pål
Familial cancer2021

Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation.

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-012-9575-x
Kuligina, Ekatherina; Sokolenko, Anna; Mitiushkina, Nathalia; Abysheva, Svetlana; Preobrazhenskaya, ...
Familial Cancer2013

Screening of HELQ in breast and ovarian cancer families

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-015-9838-4
2016

Constitutional mosaicism for aBRCA2mutation as a cause of early-onset breast cancer

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-020-00186-1
2020

Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis

Referentgranskad
DOI
10.1007/s10689-014-9773-9
2015

Hereditary leiomyomatosis and renal cell cancer (HLRCC):renal cancer risk, surveillance and treatment

Referentgranskad
DOI
10.1007/s10689-014-9735-2
2014

Can our experience with surveillance for inherited pancreatic cancer help to identify early pancreatic cancer in the general population?

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-024-00363-6
2024

Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer

Referentgranskad
DOI
10.1007/s10689-015-9778-z
2015

Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer

Referentgranskad
DOI
10.1007/s10689-012-9532-8
2012

3 '-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity

Referentgranskad
DOI
10.1007/s10689-015-9804-1
2015

Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD)

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-020-00193-2
2021

Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation.

Referentgranskad
Öppen tillgång
DOI
10.1007/s10689-012-9575-x
2013