D-Index & Metrics Best Publications
Genetics
Germany
2023

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 20,048 294 World Ranking 1290 National Ranking 98

Research.com Recognitions

Awards & Achievements

2023 - Research.com Genetics in Germany Leader Award

Overview

What is he best known for?

The fields of study Wolfgang Engel is best known for:

  • Gene
  • Enzyme
  • Spinal cord

His study on Pathology is mostly dedicated to connecting different topics, such as Degeneration (medical). His Atrophy research extends to the thematically linked field of Internal medicine. His Atrophy study frequently draws connections between related disciplines such as Internal medicine. In his study, he carries out multidisciplinary Disease and Surgery research. He undertakes interdisciplinary study in the fields of Surgery and Disease through his works. In most of his Neuroscience studies, his work intersects topics such as Saccade. Wolfgang Engel connects Saccade with Eye movement in his study. Eye movement is frequently linked to Neuroscience in his study. His Denervation research extends to the thematically linked field of Anatomy.

His most cited work include:

  • Mammalian Motor Units: Physiological-Histochemical Correlation in Three Types in Cat Gastrocnemius (723 citations)
  • Slow Saccades in Spinocerebellar Degeneration (380 citations)
  • OCULAR MOTOR ABNORMALITIES IN HEREDITARY CEREBELLAR ATAXIA (309 citations)

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

Wolfgang Engel integrates Pathology with Immunology in his research. Borrowing concepts from Pathology, he weaves in ideas under Immunology. Wolfgang Engel performs multidisciplinary study on Internal medicine and Endocrinology in his works. Wolfgang Engel integrates Endocrinology with Internal medicine in his study. Wolfgang Engel integrates Biochemistry and Enzyme in his studies. His research is interdisciplinary, bridging the disciplines of Skeletal muscle and Anatomy. Many of his studies on Skeletal muscle apply to Anatomy as well. His study deals with a combination of Disease and Pathogenesis. He combines Pathogenesis and Disease in his research.

Wolfgang Engel most often published in these fields:

  • Pathology (43.36%)
  • Internal medicine (39.82%)
  • Biochemistry (33.63%)

What were the highlights of his more recent work (between 2008-2015)?

  • Inclusion body myositis (77.78%)
  • Pathology (66.67%)
  • Myositis (66.67%)

In recent works Wolfgang Engel was focusing on the following fields of study:

In his research, Social psychology is intimately related to Inclusion (mineral), which falls under the overarching field of Mineralogy. Social psychology and Inclusion (mineral) are commonly linked in his work. Among his research on Parkinson's disease, you can see a combination of other fields of science like Parkin and Protein aggregation. Wolfgang Engel undertakes multidisciplinary investigations into Protein aggregation and Parkinson's disease in his work. He merges Inclusion body myositis with Myositis in his research. He undertakes interdisciplinary study in the fields of Myositis and Inclusion body myositis through his works. His Pathology study frequently draws connections between related disciplines such as Pathological. Wolfgang Engel regularly ties together related areas like Pathology in his Pathological studies. His work in Anatomy is not limited to one particular discipline; it also encompasses Sarcopenia.

Between 2008 and 2015, his most popular works were:

  • Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy (72 citations)
  • Sporadic inclusion-body myositis: Conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau (65 citations)
  • Pathogenic Considerations in Sporadic Inclusion-Body Myositis, a Degenerative Muscle Disease Associated With Aging and Abnormalities of Myoproteostasis (61 citations)

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

Human Y Chromosome Azoospermia Factors (AZF) Mapped to Different Subregions in Yq11

P. H. Vogt;A. Edelmann;S. Kirsch;O. Henegariu.
Human Molecular Genetics (1996)

1760 Citations

Pluripotency of spermatogonial stem cells from adult mouse testis

Kaomei Guan;Karim Nayernia;Lars S. Maier;Stefan Wagner.
Nature (2006)

1118 Citations

Targeted disruption of the Insl3 gene causes bilateral cryptorchidism.

Stephan Zimmermann;Gerd Steding;Judith M. A. Emmen;Albert O. Brinkmann.
Molecular Endocrinology (1999)

760 Citations

In Vitro-Differentiated Embryonic Stem Cells Give Rise to Male Gametes that Can Generate Offspring Mice

Karim Nayernia;Jessica Nolte;Hans W. Michelmann;Jae Ho Lee.
Developmental Cell (2006)

649 Citations

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.

Jürgen Kohlhase;Annegret Wischermann;Herbert Reichenbach;Ursula Froster.
Nature Genetics (1998)

574 Citations

Derivation of male germ cells from bone marrow stem cells

Karim Nayernia;Jae Ho Lee;Nadja Drusenheimer;Jessica Nolte.
Laboratory Investigation (2006)

423 Citations

300 million years of conserved synteny between chicken Z and human chromosome 9

Indrajit Nanda;Zhihong Shan;Manfred Schartl;Dave W. Burt.
Nature Genetics (1999)

406 Citations

Cloning of a cDNA for a novel insulin-like peptide of the testicular Leydig cells.

I M Adham;E Burkhardt;M Benahmed;W Engel.
Journal of Biological Chemistry (1993)

378 Citations

MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

R. Trappe;F. Laccone;J. Cobilanschi;M. Meins.
American Journal of Human Genetics (2001)

321 Citations

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

P. Huppke;F. Laccone;N. Krämer;W. Engel.
Human Molecular Genetics (2000)

314 Citations

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