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Enigma Consortium | Evidence-based Network for the Interpretation of Germline Mutant Alleles

Variant and data submission. ENIGMA data and results. Evidence-based Network for the. Interpretation of Germline Mutant Alleles. ENIGMA is an international consortium of investigators focused on. Determining the clinical significance of sequence variants in BRCA1, BRCA2 and other known or suspected breast cancer genes,. To provide this expert opinion to global database and classification initiatives, and. To explore optimal avenues of communication of such information at the provider and patient level.

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Enigma Consortium | Evidence-based Network for the Interpretation of Germline Mutant Alleles | enigmaconsortium.org Reviews
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Variant and data submission. ENIGMA data and results. Evidence-based Network for the. Interpretation of Germline Mutant Alleles. ENIGMA is an international consortium of investigators focused on. Determining the clinical significance of sequence variants in BRCA1, BRCA2 and other known or suspected breast cancer genes,. To provide this expert opinion to global database and classification initiatives, and. To explore optimal avenues of communication of such information at the provider and patient level.
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1 enigma consortium
2 steering committee
3 working groups
4 library
5 general documents
6 enigma publications
7 useful links
8 member login
9 meetings
10 project proposals
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Enigma Consortium | Evidence-based Network for the Interpretation of Germline Mutant Alleles | enigmaconsortium.org Reviews

https://enigmaconsortium.org

Variant and data submission. ENIGMA data and results. Evidence-based Network for the. Interpretation of Germline Mutant Alleles. ENIGMA is an international consortium of investigators focused on. Determining the clinical significance of sequence variants in BRCA1, BRCA2 and other known or suspected breast cancer genes,. To provide this expert opinion to global database and classification initiatives, and. To explore optimal avenues of communication of such information at the provider and patient level.

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ENIGMA consortium | Enigma Consortium

https://enigmaconsortium.org/documents/ENIGMA

Variant and data submission. ENIGMA data and results. ENIGMA is an international consortium of investigators focused on. Determining the clinical significance of sequence variants in BRCA1, BRCA2 and other known or suspected breast cancer genes,. To provide this expert opinion to global database and classification initiatives, and. To explore optimal avenues of communication of such information at the provider and patient level.

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bridges-research.eu bridges-research.eu

Collaborations | Bridges

https://bridges-research.eu/collaborations

Breast Cancer Association Consortium ( BCAC. Evidence-based Network for the Interpretation of Germline Mutant Alleles ( ENIGMA. Breast CAncer STratification ( B-CAST. A name chosen to reflect the compl. Exity of the exo. Orst- en eierstokkanker O. GENE SISter) a French national resource to study the missing heritability of breast cancer. German Consortium of Hereditary Breast and Ovarian Cancer. Kathleen Cuningham Foundation Consortium for Research into Familial Aspects of Breast Cancer.

nofuss.nl nofuss.nl

OPDRACHTGEVERS | NOFUSS

http://nofuss.nl/opdrachtgevers

Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door ZonMw). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door KNAW). Onderzoeksproject gesubsidieerd door CVON, Hartstichting, ZonMw en NFU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU). Zorg door en voor ouderen). Yoga aan de Vliet.

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wetenschappers | NOFUSS

http://nofuss.nl/wetenschappers

Naar de wetenschappelijke websites. Internationaal consortium van onderzoekers). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door ZonMw). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door KNAW). Onderzoeksproject gesubsidieerd door CVON, Hartstichting, ZonMw en NFU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU). Onderzoeksproject gesubsidieerd door EU).

bridges-research.eu bridges-research.eu

Bridges | Breast Cancer Risk after Diagnostic Gene Sequencing

https://bridges-research.eu/page/2

Breast Cancer Risk after Diagnostic Gene Sequencing. In this project, we aim to build a knowledge base that will allow identification of women at high-risk of breast cancer. In particular through comprehensive evaluation of DNA variants in known and suspected breast cancer genes. Exploit the huge resources established through the Breast Cancer Association Consortium ( BCAC. Evidence-based Network for the Interpretation of Germline Mutant Alleles). External Expert Advisory Board. Mirjam Plantinga has acce...

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Norwegian Group on Inherited Cancer

https://sites.google.com/site/norwgak/home

Norwegian Group on Inherited Cancer. Søk på dette nettstedet. Norsk Gruppe for Arvelig Kreft - NGAK. Norsk Gruppe for Arvelig Kreft - NGAK. Norsk Gruppe for Arvelig Kreft - NGAK. Select topics to the left, or links below. Http:/ brca.iarc.fr/. WHO classification digestive system. Norwegian Group on Inherited Cancer is a non-profit association for genetic research and clinics to describe and fight inherited cancer. CoE: Human dignity and genetic testing.

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Enigma Consortium | Evidence-based Network for the Interpretation of Germline Mutant Alleles

Variant and data submission. ENIGMA data and results. Evidence-based Network for the. Interpretation of Germline Mutant Alleles. ENIGMA is an international consortium of investigators focused on. Determining the clinical significance of sequence variants in BRCA1, BRCA2 and other known or suspected breast cancer genes,. To provide this expert opinion to global database and classification initiatives, and. To explore optimal avenues of communication of such information at the provider and patient level.

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