1999 - Royal Netherlands Academy of Arts and Sciences
Egbert Bakker works mostly in the field of Demography, limiting it down to topics relating to Population and, in certain cases, Environmental health, as a part of the same area of interest. His Environmental health study frequently links to adjacent areas such as Population. His multidisciplinary approach integrates Genetics and Genetic counseling in his work. He applies his multidisciplinary studies on Genetic counseling and Genetics in his research. Egbert Bakker integrates many fields in his works, including Gene and Allele. He undertakes multidisciplinary studies into Muscular dystrophy and Duchenne muscular dystrophy in his work. Egbert Bakker integrates several fields in his works, including Duchenne muscular dystrophy and Muscular dystrophy. Egbert Bakker performs integrative study on Internal medicine and Cardiology. He integrates Cardiology with Internal medicine in his research.
Egbert Bakker is investigating Gene as part of his Mutation, Chromosome, Locus (genetics), Genotype, Restriction fragment length polymorphism, Allele and Genetic linkage and Gene study. Egbert Bakker integrates several fields in his works, including Genotype and Gene. Egbert Bakker undertakes multidisciplinary investigations into Genetics and Molecular biology in his work. He merges Molecular biology with Genetics in his study. His Internal medicine study typically links adjacent topics like Disease. His study ties his expertise on Internal medicine together with the subject of Disease. In his articles, Egbert Bakker combines various disciplines, including Muscular dystrophy and Duchenne muscular dystrophy. Egbert Bakker carries out multidisciplinary research, doing studies in Duchenne muscular dystrophy and Muscular dystrophy. Egbert Bakker integrates Pregnancy and Fetus in his research.
Positron emission tomography is intertwined with Cerebral blood flow and Nuclear medicine in his research. With his scientific publications, his incorporates both Nuclear medicine and Positron emission tomography. By researching both Internal medicine and Pediatrics, Egbert Bakker produces research that crosses academic boundaries. He connects Pediatrics with Internal medicine in his study. He connects Genetics with Gene in his study. His work blends Gene and Genetics studies together. He performs multidisciplinary studies into Muscular dystrophy and Duchenne muscular dystrophy in his work. Egbert Bakker performs integrative study on Duchenne muscular dystrophy and Muscular dystrophy. Egbert Bakker integrates Criminology with Law in his research.
Egbert Bakker integrates Internal medicine with Pediatrics in his research. He brings together Pediatrics and Internal medicine to produce work in his papers. As part of his studies on Population, he often connects relevant subjects like Environmental health. His Environmental health study frequently involves adjacent topics like Prevalence. His Prevalence study frequently links to adjacent areas such as Population. His research on Demography frequently links to adjacent areas such as Socioeconomic status. His research on Socioeconomic status often connects related topics like Demography. Egbert Bakker integrates Muscular dystrophy with Facioscapulohumeral muscular dystrophy in his research. Egbert Bakker performs integrative study on Facioscapulohumeral muscular dystrophy and Muscular dystrophy in his works.
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AMYLOID-BETA PROTEIN-PRECURSOR GENE AND HEREDITARY CEREBRAL-HEMORRHAGE WITH AMYLOIDOSIS (DUTCH)
C. Van Broeckhoven;J. Haan;E. Bakker;J. A. Hardy.
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
J. T. Den Dunnen;P. M. Grootscholten;E. Bakker;L. A. J. Blonden.
American Journal of Human Genetics (1989)
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
A. Petrij-Bosch;T. Peelen;M. Van Vliet;R. Van Eijk.
Nature Genetics (1997)
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.
JT Wijnen;Hfa Vasen;PM Khan;AH Zwinderman.
The New England Journal of Medicine (1998)
Guidelines for diagnostic next-generation sequencing.
Gert Matthijs;Erika Souche;Mariëlle Alders;Anniek Corveleyn.
European Journal of Human Genetics (2016)
Estimating Y Chromosome Specific Microsatellite Mutation Frequencies using Deep Rooting Pedigrees
E Heyer;J Puymirat;P Dieltjes;E Bakker.
Human Molecular Genetics (1997)
Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions
M Simoni;E Bakker;M C Eurlings;Gert Matthijs.
International Journal of Andrology (1999)
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.
E Bakker;N Goor;K Wrogemann;L.M Kunkel.
The Lancet (1985)
Analysis of Molecular Variance (Amova) of Y-Chromosome-Specific Microsatellites in Two Closely Related Human Populations
L. Roewer;M. Kayser;P. Dieltjes;M. Nagy.
Human Molecular Genetics (1996)
EAA/EMQN BEST PRACTICE GUIDELINES FOR MOLECULAR DIAGNOSIS OF Y CHROMOSOMAL MICRODELETIONS
M Simoni;E Bakker.
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