Standout Papers

Rett syndrome is caused by mutations in X-linked MECP2, encod... 1985 2026 1998 2012 3.6k
  1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 (1999)
    Ruthie E. Amir, Ignatia B. Van den Veyver et al. Nature Genetics
  2. Tyrosine Kinase Receptor with Extensive Homology to EGF Receptor Shares Chromosomal Location with neu Oncogene (1985)
    Lisa M. Coussens, Teresa L. Yang‐Feng et al. Science
  3. Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand. (1987)
    Yosef Yarden, Wun-Jing Kuang et al. The EMBO Journal
  4. Structure of the receptor for platelet-derived growth factor helps define a family of closely related growth factor receptors (1986)
    Yosef Yarden, J A Escobedo et al. Nature
  5. Multiple, Distinct Forms of Bovine and Human Protein Kinase C Suggest Diversity in Cellular Signaling Pathways (1986)
    Lisa M. Coussens, Peter J. Parker et al. Science
  6. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome (1994)
    Jonathan M.J. Derry, Hans D. Ochs et al. Cell
  7. Wiskott–Aldrich Syndrome Protein, a Novel Effector for the GTPase CDC42Hs, Is Implicated in Actin Polymerization (1996)
    Marc Symons, Jonathan M.J. Derry et al. Cell
  8. Cloning, Sequencing, and Expression of the Gene Coding for the Human Platelet α 2 -Adrenergic Receptor (1987)
    Brian K. Kobilka, Hiroaki Matsui et al. Science
  9. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome (1993)
    Alejandro Aruffo, Mary Farrington et al. Cell
  10. Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion (1978)
    Vincent M. Riccardi, Eva Sujansky et al. PEDIATRICS
  11. cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor. (1987)
    Brian K. Kobilka, Richard A. F. Dixon et al. Proceedings of the National Academy of Sciences
  12. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21 (2006)
    Joseph R. Arron, Monte M. Winslow et al. Nature
  13. An intronless gene encoding a potential member of the family of receptors coupled to guanine nucleotide regulatory proteins (1987)
    Brian K. Kobilka, Thomas Frielle et al. Nature
  14. A system of nomenclature for band patterns of mouse chromosomes (1973)
    Muriel N. Nesbitt, Uta Francke Chromosoma

Immediate Impact

43 by Nobel laureates 56 from Science/Nature 97 standout
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Citing Papers

Wnt signalling in stem cells and cancer
2005 StandoutNature
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
7 intermediate papers

Works of Uta Francke being referenced

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1999 Standout
Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
1999
and 8 more

Author Peers

Author Last Decade Papers Cites
Uta Francke 23981 14319 4932 500 41.4k
Richard D. Palmiter 30313 13560 4271 470 68.2k
Paolo Sassone‐Corsi 23198 9013 3229 425 47.4k
Nancy A. Jenkins 35003 10042 6219 508 59.9k
Michael J. Owen 16227 11514 3236 603 40.0k
Michael Wigler 34084 9063 7078 217 44.8k
Robert E. Hammer 26926 10546 4234 287 52.2k
Tom Curran 31870 6616 5491 275 50.5k
James A. Richardson 35563 6106 4786 356 56.8k
Jun‐ichi Miyazaki 19214 7161 3066 494 35.6k
David E. Housman 32008 9151 9797 330 47.3k

All Works

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