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Bert Bakker

Leiden University Medical Center

13

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1532

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Monosomy 18p: Risks for developing FSHD

2016 Neuromuscular Disorders
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G.O.4

2014 Neuromuscular Disorders
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Decision Making on AUVs for adaptive minehunting surveys

2014
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Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

2012 Nature Genetics
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Genome-wide association study identifies three loci associated with melanoma risk

2009 Nature Genetics
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Y chromosome detection by Real Time PCR and pyrophosphorolysis‐activated polymerisation using free fetal DNA isolated from maternal plasma

2007 Prenatal Diagnosis
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O2: Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and arrayCGH

2005 European Journal of Medical Genetics
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Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses

2004 Human Mutation
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Combined Vascular Endothelial Growth Factor and TP53 Status Predicts Poor Response to Tamoxifen Therapy in Estrogen Receptor-positive Advanced Breast Cancer

2003 Clinical Cancer Research
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Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization

2002 American Journal of Human Genetics
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Citations (167)