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Research | 1 May 2000
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia)
- gert.matthijs@med.kuleuven.ac.be
European Journal of Human Genetics 8 , 367–371

Rights & permissionsfor article Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia) . Opens in a new window.
Research | 1 October 2002
DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)
- gert.matthijs@uz.kuleuven.ac.be
- Els Schollen
- , Kevin Martens
- , Elke Geuzens
- & Gert Matthijs
European Journal of Human Genetics 10 , 643–648

Rights & permissionsfor article DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG) . Opens in a new window.
Research | 13 August 2002
Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD)
- gert.matthijs@med.kuleuven.ac.be
European Journal of Human Genetics 10 , 505–510

Rights & permissionsfor article Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD) . Opens in a new window.
News | 22 December 2004
Research Network: EUROGLYCANET: a European network focused on congenital disorders of glycosylation
- Gert.Matthijs@med.kuleuven.ac.be
- Gert Matthijs
European Journal of Human Genetics 13 , 395–397

Rights & permissionsfor article Research Network: EUROGLYCANET: a European network focused on congenital disorders of glycosylation . Opens in a new window.
Research | 1 May 1997
Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)
- gert.matthijs@med.kuleuven.ac.be
Nature Genetics 16 , 88–92

Rights & permissionsfor article Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome) . Opens in a new window.
Reviews | 24 April 2008
Patenting and licensing in genetic testing
- gert.matthijs@uz.kuleuven.ac.be
- S Aymé
- , G Matthijs
- & S Soini
European Journal of Human Genetics 16 , S3–S9

Rights & permissionsfor article Patenting and licensing in genetic testing . Opens in a new window.
Research | 8 June 2011
Gene and genetic diagnostic method patent claims: a comparison under current European and US patent law
- Gert.Matthijs@uzleuven.be
European Journal of Human Genetics 19 , 1104–1107

Rights & permissionsfor article Gene and genetic diagnostic method patent claims: a comparison under current European and US patent law . Opens in a new window.
Editorial | 28 October 2015
New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testing
- gert.matthijs@uzleuven.be
European Journal of Human Genetics 24 , 1–1

Rights & permissionsfor article New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testing . Opens in a new window.
Research | 12 October 2005
Analysing DNA patents in relation with diagnostic genetic testing
- Gert.Matthijs@med.kuleuven.be
European Journal of Human Genetics 14 , 26–33

Rights & permissionsfor article Analysing DNA patents in relation with diagnostic genetic testing . Opens in a new window.
Research | 3 August 2011
Impact of gene patents on diagnostic testing: a new patent landscaping method applied to spinocerebellar ataxia
- gert.matthijs@uz.kuleuven.be
European Journal of Human Genetics 19 , 1114–1121

Rights & permissionsfor article Impact of gene patents on diagnostic testing: a new patent landscaping method applied to spinocerebellar ataxia . Opens in a new window.
Reviews | 24 April 2008
Patenting and licensing in genetic testing: ethical, legal and social issues
- gert.matthijs@med.kuleuven.be
European Journal of Human Genetics 16 , S10–S50

Rights & permissionsfor article Patenting and licensing in genetic testing: ethical, legal and social issues . Opens in a new window.
Reviews | 28 October 2015 | Open
Guidelines for diagnostic next-generation sequencing
- gert.matthijs@uzleuven.be
- Gert Matthijs
- , Erika Souche
- , Mariëlle Alders
- , Anniek Corveleyn
- , Sebastian Eck
- , Ilse Feenstra
- , Valérie Race
- , Erik Sistermans
- , Marc Sturm
- , Marjan Weiss
- , Helger Yntema
- , Egbert Bakker
- , Hans Scheffer
- & Peter Bauer
European Journal of Human Genetics 24 , 2–5

Rights & permissionsfor article Guidelines for diagnostic next-generation sequencing . Opens in a new window.
Reviews | 1 December 2002
European-wide opposition against the breast cancer gene patents
- Gert.Matthijs@med.kuleuven.ac.be
- Gert Matthijs
- & Dicky Halley
European Journal of Human Genetics 10 , 783–785

Rights & permissionsfor article European-wide opposition against the breast cancer gene patents . Opens in a new window.
Reviews | 24 April 2008
Introduction
- gert.matthijs@med.kuleuven.be
- Gert Matthijs
- & Ségolène Aymé
European Journal of Human Genetics 16 , S1–S2

Rights & permissionsfor article Introduction . Opens in a new window.
Comments & Opinion | 8 August 2013
The European BRCA patent oppositions and appeals: coloring inside the lines
- gert.matthijs@uzleuven.be
Nature Biotechnology 31 , 704–710

Rights & permissionsfor article The European BRCA patent oppositions and appeals: coloring inside the lines . Opens in a new window.
Comments & Opinion | 18 May 2012
The fate and future of patents on human genes and genetic diagnostic methods
- gert.matthijs@uzleuven.be
Nature Reviews Genetics 13 , 441–448

Rights & permissionsfor article The fate and future of patents on human genes and genetic diagnostic methods . Opens in a new window.
Reviews | 29 December 2005
Models for facilitating access to patents on genetic inventions
- gert.matthijs@med.kuleuven.be
Nature Reviews Genetics 7 , 143–148

Rights & permissionsfor article Models for facilitating access to patents on genetic inventions . Opens in a new window.
Comments & Opinion | 1 October 2009
Legal uncertainty in the area of genetic diagnostic testing
- gert.matthijs@uz.kuleuven.be
Nature Biotechnology 27 , 903–909

Rights & permissionsfor article Legal uncertainty in the area of genetic diagnostic testing . Opens in a new window.

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Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia)

DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)

Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD)

Research Network: EUROGLYCANET: a European network focused on congenital disorders of glycosylation

Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Patenting and licensing in genetic testing

Gene and genetic diagnostic method patent claims: a comparison under current European and US patent law

New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testing

Analysing DNA patents in relation with diagnostic genetic testing

Impact of gene patents on diagnostic testing: a new patent landscaping method applied to spinocerebellar ataxia

Patenting and licensing in genetic testing: ethical, legal and social issues

Guidelines for diagnostic next-generation sequencing

European-wide opposition against the breast cancer gene patents

Introduction

The European BRCA patent oppositions and appeals: coloring inside the lines

The fate and future of patents on human genes and genetic diagnostic methods

Models for facilitating access to patents on genetic inventions

Legal uncertainty in the area of genetic diagnostic testing

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