Thaddeus P. Dryja

Research.com Recognitions

• 1996 - Member of the National Academy of Sciences

Overview

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

  3856
  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

  2529
  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

  1253
  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

  1101
  Citations

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

  Kazuto Kajiwara;Eliot L. Berson;Thaddeus P. Dryja

  1063
  Citations

• Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.

  Margaret E. McLaughlin;Michael A. Sandberg;Eliot L. Berson;Thaddeus P. Dryja

  824
  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

  747
  Citations

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

  T Sakai;J Toguchida;N Ohtani;D W Yandell

  684
  Citations

• Point mutational inactivation of the retinoblastoma antioncogene

  Jonathan M. Horowitz;David W. Yandell;Sang-Ho Park;Susan Canning

  559
  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

  548
  Citations

• Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa

  Jane E. Olsson;Jon W. Gordon;Basil S. Pawlyk;Dorothy Roof

  546
  Citations

• Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa

  Thaddeus P. Dryja;Terri L. McGee;Lauri B. Hahn;Glenn S. Cowley

  534
  Citations

• Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.

  Thaddeus P. Dryja;Lauri B. Hahn;Glenn S. Cowley;Terri L. McGee

  521
  Citations

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

  Kazuto Kajiwara;Lauri B. Hahn;Shizuo Mukai;Gabriel H. Travis

  507
  Citations

• A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

  Philip J. Rosenfeld;Glenn S. Cowley;Terri L. McGee;Michael A. Sandberg

  490
  Citations

• Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness.

  Thaddeus P. Dryja;Eliot L. Berson;Vikram R. Rao;Daniel D. Oprian

  439
  Citations

• Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns

  Carlo Rivolta;Dror Sharon;Margaret M. DeAngelis;Thaddeus P. Dryja

  411
  Citations

• Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa

  Margaret E. McLaughlin;Traci L. Ehrhart;Eliot L. Berson;Thaddeus P. Dryja

  407
  Citations

• Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis

  Thaddeus P. Dryja;Scott M. Adams;Jonna L. Grimsby;Terri L. McGee

  393
  Citations

• Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa.

  Thaddeus P. Dryja;John T. Finn;You Wei Peng;Terri L. Mcgee

  385
  Citations