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Uta Francke

Active 1972–2016

181
Papers
46,020
Citations
115
h-index
181
i10-index

Citations

Citations per year for Uta Francke1966: 1 citations1974: 1 citations1975: 5 citations1976: 3 citations1977: 10 citations1978: 18 citations1979: 24 citations1980: 21 citations1981: 31 citations1982: 58 citations1983: 61 citations1984: 94 citations1985: 98 citations1986: 144 citations1987: 257 citations1988: 336 citations1989: 342 citations1990: 378 citations1991: 342 citations1992: 382 citations1993: 358 citations1994: 396 citations1995: 326 citations1996: 427 citations1997: 380 citations1998: 448 citations1999: 470 citations2000: 508 citations2001: 468 citations2002: 452 citations2003: 382 citations2004: 298 citations2005: 290 citations2006: 311 citations2007: 254 citations2008: 286 citations2009: 327 citations2010: 288 citations2011: 258 citations2012: 246 citations2013: 265 citations2014: 299 citations2015: 214 citations2016: 223 citations2017: 195 citations2018: 191 citations2019: 566 citations2020: 552 citations2021: 490 citations2022: 334 citations2023: 212 citations2024: 341 citations2025: 100 citations2026: 2 citations1967–1973: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,443 citing papers, 38.9% of this breakdownUnited Kingdom: 1,349 citing papers, 8.1% of this breakdownGermany: 956 citing papers, 5.8% of this breakdownJapan: 776 citing papers, 4.7% of this breakdownFrance: 743 citing papers, 4.5% of this breakdownCanada: 680 citing papers, 4.1% of this breakdownItaly: 661 citing papers, 4% of this breakdownChina: 496 citing papers, 3% of this breakdownNetherlands: 481 citing papers, 2.9% of this breakdownAustralia: 448 citing papers, 2.7% of this breakdownSwitzerland: 362 citing papers, 2.2% of this breakdownSpain: 318 citing papers, 1.9% of this breakdown
0%38.9%Other 17.2%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology52.5%
  • Medicine29.7%
  • Neuroscience8.1%
  • Immunology and Microbiology6.8%
  • Agricultural and Biological Sciences1.1%
  • Nursing0.3%
  • Other1.5%

Topics

  • Genetics and Neurodevelopmental Disorders4.6%
  • Epigenetics and DNA Methylation2.8%
  • Autism Spectrum Disorder Research2%
  • Receptor Mechanisms and Signaling1.7%
  • Cell Adhesion Molecules Research1.5%
  • RNA modifications and cancer1.5%
  • Other85.9%

Coauthors

All papers

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  1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

    Authors: Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan, Charles Q. Tran, Uta Francke, Huda Y. Zoghbi - Nature Genetics 1999 cited by 5,028

  2. Identification of a Gene (GPR30) with Homology to the G-Protein-Coupled Receptor Superfamily Associated with Estrogen Receptor Expression in Breast Cancer

    Authors: Charles Carmeci, Devon A. Thompson, Huijun Z. Ring, Uta Francke, Ronald J. Weigel - Genomics 1997 cited by 578

  3. Widespread changes in dendritic and axonal morphology in Mecp2‐mutant mouse models of rett syndrome: Evidence for disruption of neuronal networks

    Authors: Pavel V. Belichenko, Elena E. Wright, Nadia P. Belichenko, Eliezer Masliah, Hong Hua Li, William C. Mobley, Uta Francke - The Journal of Comparative Neurology 2009 cited by 277

  4. Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms

    Authors: David A. Hinds, Kimberly E. Barnholt, Ruben A. Mesa, Amy K. Kiefer, Chuong B. Do, Nicholas Eriksson, Joanna L. Mountain, Uta Francke, Joyce Y. Tung, Huong Nguyen, Haiyu Zhang, Linda Gojenola, James L. Zehnder, Jason Gotlib - Blood 2016 cited by 268

  5. Tyrosine Kinase Receptor with Extensive Homology to EGF Receptor Shares Chromosomal Location with neu Oncogene

    Authors: Lisa M. Coussens, Teresa L. Yang‐Feng, Yu-Cheng Liao, Ellson Chen, Alane Gray, John P. McGrath, Peter H. Seeburg, Towia A. Libermann, Joseph Schlessinger, Uta Francke, Arthur D. Levinson, Axel Ullrich - Science 1985 cited by 1,799

  6. Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease

    Authors: Chuong B. Do, Joyce Y. Tung, Elizabeth H. Dorfman, Amy K. Kiefer, Emily M. Drabant, Uta Francke, Joanna L. Mountain, Samuel M. Goldman, Caroline M. Tanner, J. William Langston, Anne Wojcicki, Nicholas Eriksson - PLoS Genetics 2011 cited by 534

  7. Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots

    Authors: Mimi Wan, Stephen Sung Jae Lee, Xianyu Zhang, Elisa J. F. Houwink, Hae-Ri Song, Ruthie E. Amir, Sarojini Budden, Sakkubai Naidu, José Luiz Pinto Pereira, Ivan F. M. Lo, Huda Y. Zoghbi, N. Carolyn Schanen, Uta Francke - The American Journal of Human Genetics 1999 cited by 518

  8. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21

    Authors: Joseph R. Arron, Monte M. Winslow, Alberto Polleri, Ching-Pin Chang, Haiyan Wu, Xin Gao, Joel R. Neilson, Lei Chen, Jeremy J. Heit, Seung K. Kim, Nobuyuki Yamasaki, Tsuyoshi Miyakawa, Uta Francke, Isabella A. Graef, Gerald R. Crabtree - Nature 2006 cited by 703

  9. Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia

    Authors: Amy K. Kiefer, Joyce Y. Tung, Chuong B. Do, David A. Hinds, Joanna L. Mountain, Uta Francke, Nicholas Eriksson - PLoS Genetics 2013 cited by 315

  10. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

    Authors: Jonathan M.J. Derry, Hans D. Ochs, Uta Francke - Cell 1994 cited by 1,058

  11. Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study

    Authors: Laurence Faivre, Gwenaëlle Collod‐Béroud, Bart Loeys, Anne H. Child, Christine Binquet, Élodie Gautier, Bert Callewaert, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Anatoli Kiotsekoglou, Paolo Comeglio, Nicola Marziliano, Harry C. Dietz, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, Christine Muti, Henri Plauchu, Peter N. Robinson, Lesley C. Adès, Andrew Biggin, B. Benetts, Maggie Brett, Katherine Holman, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Guillaume Jondeau, Cathérine Boileau - The American Journal of Human Genetics 2007 cited by 603

  12. SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice

    Authors: Feng Ding, Hong Hua Li, Shengwen Zhang, Nicola M. Solomon, Sally A. Camper, Pinchas Cohen, Uta Francke - PLoS ONE 2008 cited by 288

  13. Cardiovascular manifestations in men and women carrying a FBN1 mutation

    Authors: Delphine Détaint, Laurence Faivre, Gwenaëlle Collod‐Béroud, Anne H. Child, Bart Loeys, Christine Binquet, Élodie Gautier, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Chantal Stheneur, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, Henri Plauchu, Peter N. Robinson, Anatoli Kiotsekoglou, Julie De Backer, Lesley C. Adès, Uta Francke, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau - European Heart Journal 2010 cited by 162

  14. Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie cerebrotendinous xanthomatosis.

    Authors: James J. Cali, C L Hsieh, Uta Francke, David W. Russell - Journal of Biological Chemistry 1991 cited by 504

  15. Molecular analysis and chromosomal mapping of amplified genes isolated from a transformed mouse 3T3 cell line

    Authors: Linda Cahilly-Snyder, Teresa L. Yang‐Feng, Uta Francke, Donna L. George - Somatic Cell and Molecular Genetics 1987 cited by 359

  16. A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci

    Authors: David A. Hinds, George McMahon, Amy K. Kiefer, Chuong B Do, Nicholas Eriksson, David M. Evans, Beaté St Pourcain, Susan M. Ring, Joanna L. Mountain, Uta Francke, George Davey-Smith, Nicholas J. Timpson, Joyce Y. Tung - Nature Genetics 2013 cited by 250

  17. Control of bone formation by the serpentine receptor Frizzled-9

    Authors: Joachim Albers, Jochen Schulze, Frank Timo Beil, Matthias Gebauer, Anke Baranowsky, Johannes Keller, Robert Percy Marshall, Kristofer Wintges, Felix W. Friedrich, Matthias Priemel, Arndt F. Schilling, Johannes M. Rueger, Kerstin Cornils, Boris Fehse, Thomas Streichert, Guido Sauter, Franz Jakob, Karl Insogna, Barbara R. Pober, Klaus‐Peter Knobeloch, Uta Francke, Michael Amling, Thorsten Schinke - The Journal of Cell Biology 2011 cited by 112

  18. Wiskott–Aldrich Syndrome Protein, a Novel Effector for the GTPase CDC42Hs, Is Implicated in Actin Polymerization

    Authors: Marc Symons, Jonathan M.J. Derry, Brian Karlak, Sharon Jiang, Vanessa Lemahieu, Frank McCormick, Uta Francke, Arie Abo - Cell 1996 cited by 861

  19. Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci

    Authors: Nicholas Eriksson, Joyce Y. Tung, Amy K. Kiefer, David A. Hinds, Uta Francke, Joanna L. Mountain, Chuong B. Do - PLoS ONE 2012 cited by 153

  20. Efficient Replication of over 180 Genetic Associations with Self-Reported Medical Data

    Authors: Joyce Y. Tung, Chuong B. Do, David A. Hinds, Amy K. Kiefer, J. Michael Macpherson, Arnab B. Chowdry, Uta Francke, Brian Naughton, Joanna L. Mountain, Anne Wojcicki, Nicholas Eriksson - PLoS ONE 2011 cited by 147

  21. Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation

    Authors: Birgitt Schüle, Angélica Oviedo, Kathreen Johnston, Shashidhar Pai, Uta Francke - The American Journal of Human Genetics 2005 cited by 147

  22. A genetic variant near olfactory receptor genes influences cilantro preference

    Authors: Nicholas Eriksson, Shirley Wu, Chuong B Do, Amy K. Kiefer, Joyce Y. Tung, Joanna L. Mountain, David A. Hinds, Uta Francke - Flavour 2012 cited by 119

  23. Genetic variants associated with breast size also influence breast cancer risk

    Authors: Nicholas Eriksson, Geoffrey Marsing Benton, Chuong B Do, Amy K. Kiefer, Joanna L. Mountain, David A. Hinds, Uta Francke, Joyce Y. Tung - BMC Medical Genetics 2012 cited by 84

  24. Human proto‐oncogene c‐kit: a new cell surface receptor tyrosine kinase for an unidentified ligand.

    Authors: Yosef Yarden, Wun-Jing Kuang, Teresa L. Yang‐Feng, Lisa M. Coussens, S Munemitsu, Thomas J. Dull, Edith Wen-Chu Chen, Joseph Schlessinger, Uta Francke, A. Ullrich - The EMBO Journal 1987 cited by 1,599