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 and Molecular Biology D-index 84 Citations 30,554 168 World Ranking 826 National Ranking 457

Research.com Recognitions

Awards & Achievements

1996 - Member of the National Academy of Sciences

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

His scientific interests lie mostly in Genetics, Retinitis pigmentosa, Gene, Mutation and Molecular biology. As part of his studies on Genetics, he often connects relevant areas like Rhodopsin. He has researched Rhodopsin in several fields, including Congenital stationary night blindness, Mutant and Transversion.

His Retinitis pigmentosa research integrates issues from Retinal degeneration, Missense mutation, Electroretinography and Visual phototransduction. His Molecular biology research includes elements of Retina and Exon. Thaddeus P. Dryja has included themes like Chromosome 13, Cancer research, Germline mutation and Somatic cell in his Retinoblastoma study.

His most cited work include:

  • A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma (2374 citations)
  • Expression of recessive alleles by chromosomal mechanisms in retinoblastoma (1642 citations)
  • A point mutation of the rhodopsin gene in one form of retinitis pigmentosa (865 citations)

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

His primary areas of study are Genetics, Retinitis pigmentosa, Gene, Molecular biology and Mutation. His study involves Allele, Locus, Missense mutation, Exon and Retinoblastoma, a branch of Genetics. The study incorporates disciplines such as Chromosome 13, Cancer research, DNA and Retinoblastoma gene in addition to Retinoblastoma.

His Retinitis pigmentosa study integrates concerns from other disciplines, such as Retinal degeneration, Rhodopsin and Electroretinography. His Rhodopsin research is multidisciplinary, relying on both Retina and Mutant. Molecular biology is frequently linked to Gene mutation in his study.

He most often published in these fields:

  • Genetics (46.34%)
  • Retinitis pigmentosa (28.66%)
  • Gene (27.13%)

What were the highlights of his more recent work (between 2009-2021)?

  • Pathology (13.11%)
  • Ophthalmology (15.55%)
  • Gene (27.13%)

In recent papers he was focusing on the following fields of study:

His primary scientific interests are in Pathology, Ophthalmology, Gene, Retina and Pharmacology. His studies deal with areas such as Hyaluronic acid, Dermal Fillers, PAX8 and Eyelid as well as Pathology. His work carried out in the field of Ophthalmology brings together such families of science as Animal model, Psychiatry and Age related.

His Gene study contributes to a more complete understanding of Genetics. Thaddeus P. Dryja interconnects Complement system, Viral vector, Nucleic acid and Cancer research in the investigation of issues within Retina. He combines subjects such as Antibody, Neutralizing antibody and Bioinformatics with his study of Pharmacology.

Between 2009 and 2021, his most popular works were:

  • Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis (771 citations)
  • Supplementary Materials for Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis (156 citations)
  • Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa (104 citations)

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

  • Gene
  • Mutation
  • Genetics

His primary areas of investigation include Gene, Genetics, Internal medicine, Antibody and Psoriasis. His Gene research is multidisciplinary, incorporating perspectives in Retina, Nucleic acid and Virology. His work is connected to Retinitis pigmentosa, Linkage disequilibrium, Haplotype, Single-nucleotide polymorphism and Minor allele frequency, as a part of Genetics.

His work deals with themes such as Sensorineural hearing loss and Mutation, Frameshift mutation, Exon, which intersect with Retinitis pigmentosa. His Antibody research includes themes of Receptor, Retinal, Pharmacology and Peptide. His Psoriasis research is multidisciplinary, incorporating elements of Rheumatoid arthritis, Uveitis and Rheumatology.

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

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

Stephen H. Friend;Stephen H. Friend;Rene Bernards;Snezna Rogelj;Robert A. Weinberg.
Nature (1986)

3572 Citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

W. K. Cavenee;W. K. Cavenee;T. P. Dryja;R. A. Phillips;William F Benedict.
Nature (1983)

2403 Citations

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Thaddeus P. Dryja;Terri L. McGee;Elias Reichel;Lauri B. Hahn.
Nature (1990)

1175 Citations

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

Kazuto Kajiwara;Eliot L. Berson;Thaddeus P. Dryja.
Science (1994)

1016 Citations

Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis

Wolfgang Hueber;Dhavalkumar D Patel;Thaddeus Dryja;Andrew M Wright.
Science Translational Medicine (2010)

978 Citations

Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa

Margaret E. McLaughlin;Michael A. Sandberg;Eliot L. Berson;Thaddeus P. Dryja.
Nature Genetics (1993)

781 Citations

Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells.

Jonathan M. Horowitz;Sang Ho Park;Emil Bogenmann;Jeng Chung Cheng;Jeng Chung Cheng.
Proceedings of the National Academy of Sciences of the United States of America (1990)

704 Citations

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

Kazuto Kajiwara;Lauri B. Hahn;Shizuo Mukai;Gabriel H. Travis.
Nature (1991)

661 Citations

Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene.

T Sakai;J Toguchida;N Ohtani;D W Yandell.
American Journal of Human Genetics (1991)

657 Citations

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis

Hiroyuki Morimura;Gerald A. Fishman;Sandeep A. Grover;Anne B. Fulton.
Proceedings of the National Academy of Sciences of the United States of America (1998)

515 Citations

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