Brendan Lee

Active 1989–2025

173
Papers
22,190
Citations
87
h-index
161
i10-index

Citations

Citations per year for Brendan Lee1964: 1 citations1989: 1 citations1990: 11 citations1991: 8 citations1992: 19 citations1993: 22 citations1994: 24 citations1995: 34 citations1996: 22 citations1997: 29 citations1998: 33 citations1999: 51 citations2000: 67 citations2001: 60 citations2002: 74 citations2003: 90 citations2004: 74 citations2005: 62 citations2006: 87 citations2007: 66 citations2008: 122 citations2009: 134 citations2010: 151 citations2011: 161 citations2012: 154 citations2013: 168 citations2014: 172 citations2015: 173 citations2016: 190 citations2017: 178 citations2018: 189 citations2019: 759 citations2020: 824 citations2021: 801 citations2022: 616 citations2023: 474 citations2024: 783 citations2025: 320 citations2026: 11 citations1965–1988: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,925 citing papers, 30.1% of this breakdownChina: 1,042 citing papers, 10.7% of this breakdownUnited Kingdom: 606 citing papers, 6.2% of this breakdownGermany: 589 citing papers, 6.1% of this breakdownCanada: 403 citing papers, 4.1% of this breakdownItaly: 369 citing papers, 3.8% of this breakdownFrance: 365 citing papers, 3.8% of this breakdownNetherlands: 310 citing papers, 3.2% of this breakdownJapan: 309 citing papers, 3.2% of this breakdownAustralia: 279 citing papers, 2.9% of this breakdownSpain: 179 citing papers, 1.8% of this breakdownSwitzerland: 174 citing papers, 1.8% of this breakdown
0%30.1%Other 22.3%

Fields

  • Biochemistry, Genetics and Molecular Biology61.2%
  • Medicine29.7%
  • Neuroscience3.4%
  • Immunology and Microbiology1.8%
  • Engineering1%
  • Computer Science0.9%
  • Other2%

Topics

  • Connective tissue disorders research3.6%
  • Genomics and Rare Diseases3.3%
  • Bone Metabolism and Diseases2.8%
  • Genomic variations and chromosomal abnormalities1.9%
  • Bone health and treatments1.8%
  • Osteoarthritis Treatment and Mechanisms1.7%
  • Other84.9%

Coauthors

All papers

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  1. Impairment of an Endothelial NAD+-H2S Signaling Network Is a Reversible Cause of Vascular Aging

    Authors: , , , , , , , , , , , , , , , , , , , , , - Cell 2018 cited by 508

  2. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael F. Wangler, Monte Westerfield, Matthew T. Wheeler, Anastasia L. Wise, Elizabeth A. Worthey, Shinya Yamamoto, Euan A. Ashley - New England Journal of Medicine 2018 cited by 374

  3. Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing

    Authors: , , , , , , , , , , , , , , , , , - Journal of Clinical Investigation 2020 cited by 188

  4. The Osteogenic Niche Promotes Early-Stage Bone Colonization of Disseminated Breast Cancer Cells

    Authors: , , , , , , , , , , , , , , , , - Cancer Cell 2015 cited by 386

  5. Targeting TGF-β for treatment of osteogenesis imperfecta

    Authors: , , , , , , , , , , , , , , , , , , , , - Journal of Clinical Investigation 2022 cited by 82

  6. Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta

    Authors: , , , , , , , , , , , , , , , , - Nature Medicine 2014 cited by 304

  7. Use of Exome Sequencing for Infants in Intensive Care Units

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jianhong Hu, John W. Belmont, Lindsay C. Burrage, Brett H. Graham, V. Reid Sutton, William J. Craigen, Sharon E. Plon, James R. Lupski, Arthur L. Beaudet, Richard A. Gibbs, Donna M. Muzny, Marcus J. Miller, Xia Wang, Magalie S. Leduc, Rui Xiao, Pengfei Liu, Chad A. Shaw, Magdalena Walkiewicz, Weimin Bi, Fan Xia, Brendan Lee, Christine M. Eng, Yaping Yang, Seema R. Lalani - JAMA Pediatrics 2017 cited by 431

  8. Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carlos E. Prada, Jong‐Hee Chae, Tiphanie P. Vogel, Hugo J. Bellen - Neuron 2020 cited by 163

  9. TGF-β Family Signaling in Mesenchymal Differentiation

    Authors: , , , , , , - Cold Spring Harbor Perspectives in Biology 2017 cited by 266

  10. Die Rolle von .NET als Application Server

    Authors: , , , , , , , , , - Blood 2004 cited by 233

  11. Identification of Functionally Distinct Mx1+αSMA+ Periosteal Skeletal Stem Cells

    Authors: , , , , , , , , , , , - Cell stem cell 2019 cited by 195

  12. Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation

    Authors: , , , , , , , , , , , , - Journal of Clinical Investigation 2020 cited by 82

  13. Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nienke E. Verbeek, Magdalena Walkiewicz, Elaine H. Zackai, Christiane Zweier, Martin Zenker, Brendan Lee, Leslie G. Biesecker - Genetics in Medicine 2018 cited by 220

  14. Leukocyte-Rich Platelet-Rich Plasma Is Predominantly Anti-inflammatory Compared With Leukocyte-Poor Platelet-Rich Plasma in Patients With Mild-Moderate Knee Osteoarthritis: A Prospective, Descriptive Laboratory Study

    Authors: , , , , - The American Journal of Sports Medicine 2023 cited by 60

  15. WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta

    Authors: , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2013 cited by 356

  16. Evaluation of teriparatide treatment in adults with osteogenesis imperfecta

    Authors: , , , , , , , , , , , - Journal of Clinical Investigation 2014 cited by 213

  17. AI-MARRVEL — A Knowledge-Driven AI System for Diagnosing Mendelian Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , - NEJM AI 2024 cited by 43

  18. Mitochondrial uncoupler BAM15 reverses diet-induced obesity and insulin resistance in mice

    Authors: , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2020 cited by 135

  19. Gene therapy for repair and regeneration of bone and cartilage

    Authors: , - Current Opinion in Pharmacology 2018 cited by 83

  20. CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta

    Authors: , , , , , , , , , , , , , , , , , , , - Cell 2006 cited by 533

  21. Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory Syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2018 cited by 168

  22. Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis

    Authors: , , , - Biomolecules 2020 cited by 85

  23. Dimorphic effects of Notch signaling in bone homeostasis

    Authors: , , , , , , , , , , , - Nature Medicine 2008 cited by 418

  24. Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis

    Authors: , , , , , , , - Journal of Clinical Investigation 2017 cited by 179