D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 74 Citations 16,170 244 World Ranking 1309 National Ranking 44

Research.com Recognitions

Awards & Achievements

1999 - Royal Netherlands Academy of Arts and Sciences

Overview

What is he best known for?

The fields of study Egbert Bakker is best known for:

  • Gene
  • DNA
  • Mutation

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.

His most cited work include:

  • Amyloid β Protein Precursor Gene and Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch) (432 citations)
  • BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients (399 citations)
  • EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004 (394 citations)

What are the main themes of his work throughout his whole career to date

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.

Egbert Bakker most often published in these fields:

  • Genetics (71.03%)
  • Gene (64.83%)
  • Internal medicine (33.10%)

What were the highlights of his more recent work (between 2010-2019)?

  • Internal medicine (63.16%)
  • Genetics (31.58%)
  • Gene (21.05%)

In recent works Egbert Bakker was focusing on the following fields of study:

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.

Between 2010 and 2019, his most popular works were:

  • Population-based incidence and prevalence of facioscapulohumeral dystrophy (240 citations)
  • Accuracy and precision of pseudo-continuous arterial spin labeling perfusion during baseline and hypercapnia: A head-to-head comparison with 15O H2O positron emission tomography (120 citations)
  • Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy (53 citations)

In his most recent research, the most cited works focused on:

  • Rheumatoid arthritis
  • Gene
  • Muscular dystrophy

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

AMYLOID-BETA PROTEIN-PRECURSOR GENE AND HEREDITARY CEREBRAL-HEMORRHAGE WITH AMYLOIDOSIS (DUTCH)

C. Van Broeckhoven;J. Haan;E. Bakker;J. A. Hardy.
Science (1990)

662 Citations

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)

652 Citations

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)

501 Citations

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)

492 Citations

Guidelines for diagnostic next-generation sequencing.

Gert Matthijs;Erika Souche;Mariëlle Alders;Anniek Corveleyn.
European Journal of Human Genetics (2016)

476 Citations

Estimating Y Chromosome Specific Microsatellite Mutation Frequencies using Deep Rooting Pedigrees

E Heyer;J Puymirat;P Dieltjes;E Bakker.
Human Molecular Genetics (1997)

375 Citations

Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions

M Simoni;E Bakker;M C Eurlings;Gert Matthijs.
International Journal of Andrology (1999)

372 Citations

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)

348 Citations

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)

280 Citations

EAA/EMQN BEST PRACTICE GUIDELINES FOR MOLECULAR DIAGNOSIS OF Y CHROMOSOMAL MICRODELETIONS

M Simoni;E Bakker.
(2004)

266 Citations

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