Research Explorer

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Researcher

Petra Van Acker

Awards & Distinctions

12 Results

2015

Comparison of methods for in-house screening of HLA*B57:01 to prevent abacavir hypersensitivity in HIV-1 care

Ward De SpiegelaereJan PhilippéKAREN VERVISCHChris VerhofstedeEva MalatinkováMaja KiselinovaWim TrypsteenPawel BonczkowskiDirk VogelaersSteven Callens et al.

A1 Journal Article in PLOS ONE

2012

Characterization of LEDGF/p75 genetic variants and association with HIV-1 disease progression

Peter MessiaenWard De SpiegelaereJose AlcamiKaren VervischPetra Van AckerBruno VerhasseltPieter MeuwissenEsther CalongeNuria GonzalezFelix Gutierrez-Rodero et al.

A1 Journal Article in PLOS ONE

Comprehensive characterization of LEDGF/p75 in a HIV-1 infected patient cohort

Peter MessiaenWard De SpiegelaereJose AlcamiPaul CouckePetra Van AckerKaren VervischBruno VerhasseltPieter MeeuwissenBruce PoppeDirk Vogelaers et al.

2011

Comprehensive characterization of LEDGF/p75 in a HIV-1-infected patient cohort

Peter MessiaenWard De SpiegelaereChris VerhofstedePaul CouckePetra Van AckerPhilip VlummensKAREN VERVISCHDirk VogelaersBruce PoppeJose Alcami et al.

2008

Novel clinico-molecular insights in Pseudoxanthoma elasticum provide an efficient molecular screening method and a comprehensive diagnostic flowchart

Olivier VanakkerBart LeroyPaul CouckeLionel G BercovitchJouni UittoDennis ViljoenSharon F TerryPetra Van AckerDirk MatthysBart Loeys et al.

A2 Journal Article in HUMAN MUTATION

2006

Mutation analysis in the FBN1 gene in patients with Marfan Syndrome

Paul CouckePetra Van AckerAnne De Paepe

Bookchapter in Congenital Heart Diseases

Mutation analysis of the FBN1 gene in patients with Marfan syndrome

Paul CouckePetra Van AckerAnne De Paepe

A4 Journal Article in METHODS IN MOLECULAR MEDICINE

2004

Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome

Bart LoeysJulie De BackerPetra Van AckerKaren WettinckG PALSLieve NuytinckPaul CouckeAnne De Paepe

A1 Journal Article in HUMAN MUTATION

2003

Homozygosity mapping of a gene for arterial tortuosity snydrome

Paul CouckeNW WESSELSPetra Van AckerR GARDELLAS BARLATIPJ WILLEMSM COLOMBIAnne De Paepe

Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13

Paul CouckeMW WesselsPetra Van AckerR GardellaS BarlatiPJ WillemsM ColombiAnne De Paepe

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

2002

Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).

Bart LoeysLieve NuytinckPetra Van AckerSOPHIE WALRAEDTM BONDUELLEK SERMONB HAMELA SANCHEZLudwine MessiaenAnne De Paepe

A1 Journal Article in PRENATAL DIAGNOSIS

2001

Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient.

R GARDELLALieve NuytinckS BARLATIPetra Van AckerG TADINIAnne De PaepeM COLOMBI

A1 Journal Article in CLINICAL AND EXPERIMENTAL DERMATOLOGY