Norman Arnheim

Active 1967–2012

76
Papers
28,021
Citations
70
h-index
73
i10-index

Citations

Citations per year for Norman Arnheim1968: 1 citations1969: 2 citations1970: 2 citations1971: 3 citations1972: 6 citations1973: 3 citations1974: 8 citations1975: 9 citations1976: 2 citations1977: 1 citations1978: 3 citations1979: 12 citations1980: 11 citations1981: 20 citations1982: 23 citations1983: 12 citations1984: 26 citations1985: 25 citations1986: 40 citations1987: 49 citations1988: 154 citations1989: 326 citations1990: 424 citations1991: 402 citations1992: 337 citations1993: 277 citations1994: 253 citations1995: 220 citations1996: 220 citations1997: 231 citations1998: 214 citations1999: 237 citations2000: 238 citations2001: 193 citations2002: 208 citations2003: 239 citations2004: 200 citations2005: 167 citations2006: 169 citations2007: 167 citations2008: 170 citations2009: 144 citations2010: 176 citations2011: 139 citations2012: 122 citations2013: 111 citations2014: 111 citations2015: 115 citations2016: 81 citations2017: 72 citations2018: 79 citations2019: 209 citations2020: 225 citations2021: 178 citations2022: 140 citations2023: 80 citations2024: 171 citations2025: 61 citations2026: 1 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,365 citing papers, 40.5% of this breakdownUnited Kingdom: 718 citing papers, 8.6% of this breakdownGermany: 551 citing papers, 6.6% of this breakdownJapan: 389 citing papers, 4.7% of this breakdownFrance: 337 citing papers, 4.1% of this breakdownCanada: 284 citing papers, 3.4% of this breakdownChina: 270 citing papers, 3.3% of this breakdownItaly: 218 citing papers, 2.6% of this breakdownAustralia: 185 citing papers, 2.2% of this breakdownSpain: 183 citing papers, 2.2% of this breakdownNetherlands: 176 citing papers, 2.1% of this breakdownSweden: 156 citing papers, 1.9% of this breakdown
0%40.5%Other 17.8%

Fields

  • Biochemistry, Genetics and Molecular Biology48.1%
  • Medicine31.6%
  • Neuroscience5.2%
  • Immunology and Microbiology4.7%
  • Agricultural and Biological Sciences3.7%
  • Environmental Science1.9%
  • Other4.8%

Topics

  • Mitochondrial Function and Pathology3.8%
  • DNA Repair Mechanisms3.2%
  • RNA and protein synthesis mechanisms2.3%
  • Genetic Neurodegenerative Diseases2%
  • Advanced biosensing and bioanalysis techniques2%
  • CRISPR and Genetic Engineering2%
  • Other84.7%

Coauthors

All papers

Open in search
  1. Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia

    Authors: , , , , , , - Science 1985 cited by 9,022

  2. Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over

    Authors: , , , , , , , , , , , - Nature Genetics 1996 cited by 834

  3. Detection of a specific mitochondrial DNA deletion in tissues of older humans

    Authors: , - Nucleic Acids Research 1990 cited by 792

  4. Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain

    Authors: , , , , , , , , , - Human Molecular Genetics 2007 cited by 231

  5. Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes

    Authors: , , , , , - Cell 1988 cited by 2,115

  6. Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B

    Authors: , , , - PLoS Genetics 2012 cited by 75

  7. Whole genome amplification from a single cell: implications for genetic analysis.

    Authors: , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 1992 cited by 902

  8. Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm

    Authors: , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2006 cited by 398

  9. Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DMA mismatch repair

    Authors: , , , , , , , , , , , , - Nature Genetics 1998 cited by 364

  10. A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues.

    Authors: , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 1992 cited by 640

  11. Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

    Authors: , , , - Nature Genetics 1992 cited by 419

  12. Understanding what determines the frequency and pattern of human germline mutations

    Authors: , - Nature Reviews Genetics 2009 cited by 140

  13. Polyglutamine-Expanded Human Huntingtin Transgenes Induce Degeneration of Drosophila Photoreceptor Neurons

    Authors: , , , , , , , - Neuron 1998 cited by 529

  14. Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

    Authors: , , , , , , , , , , , - Cell 1995 cited by 534

  15. Deleterious mitochondrial DNA mutations accumulate in aging human tissues

    Authors: , - Mutation Research/DNAging 1992 cited by 216

  16. The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect

    Authors: , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2002 cited by 166

  17. Contributions by MutL Homologues Mlh3 and Pms2 to DNA Mismatch Repair and Tumor Suppression in the Mouse

    Authors: , , , , , , , , , , - Cancer Research 2005 cited by 97

  18. A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations

    Authors: , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2008 cited by 91

  19. The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes

    Authors: , , , , , , , - PLoS Biology 2007 cited by 76

  20. Extension of base mispairs byTaqDNA polymerase: implications for single nucleotide discrimination in PCR

    Authors: , , - Nucleic Acids Research 1992 cited by 370

  21. Differential Contributions of Mammalian Rad54 Paralogs to Recombination, DNA Damage Repair, and Meiosis

    Authors: , , , , , , , , , , , , , , , , , , , , - Molecular and Cellular Biology 2006 cited by 158

  22. Nup50, a Nucleoplasmically Oriented Nucleoporin with a Role in Nuclear Protein Export

    Authors: , , , , , , , - Molecular and Cellular Biology 2000 cited by 141

  23. Different mutator phenotypes in Mlh1 - versus Pms2 -deficient mice

    Authors: , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 1999 cited by 137

  24. Huntington disease expansion mutations in humans can occur before meiosis is completed

    Authors: , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2003 cited by 104