Norman Arnheim
Active 1967–2012
- 76
- Papers
- 28,021
- Citations
- 70
- h-index
- 73
- i10-index
Citations
Citation sources
Countries
Institutions
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
- Darryl Shibata9
- Peter Calabrese7
- Song‐Ro Yoon6
- Allan C. Wilson5
- Gino Cortopassi5
- Henry A. Erlich5
- Irene Tiemann‐Boege5
- Martin Wj5
- R. Michael Liskay5
- Lin Zhang4
- Randall K. Saiki4
- Sean M. Baker4
- William Navidi4
- Xiang Yao4
- Christian Bronner3
- Karin Schmitt3
- Marcy E. MacDonald3
- Nancy S. Wexler3
- René Hubert3
- Soo‐Kyung Choi3
- Tomas A. Prolla3
- Allan Bradley2
- Allie C. Harris2
- Andrew J. Wyrobek2
All papers
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
Authors: Randall K. Saiki, Stephen J. Scharf, Fred Faloona, Kary B. Mullis, Glenn T. Horn, Henry A. Erlich, Norman Arnheim - Science 1985 cited by 9,022
- Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
Authors: Sean M. Baker, Annemieke W. Plug, Tomas A. Prolla, Christian Bronner, Allie C. Harris, Xiang Yao, D M Christie, Craig Monell, Norman Arnheim, Allan Bradley, Terry Ashley, R. Michael Liskay - Nature Genetics 1996 cited by 834
- Detection of a specific mitochondrial DNA deletion in tissues of older humans
Authors: Gino Cortopassi, Norman Arnheim - Nucleic Acids Research 1990 cited by 792
- Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain
Authors: Peggy Shelbourne, Christine E. Keller-McGandy, Wenya Linda Bi, Song‐Ro Yoon, Louis Dubeau, Nicola Veitch, Jean Paul Vonsattel, Nancy S. Wexler, Norman Arnheim, Sarah J. Augood - Human Molecular Genetics 2007 cited by 231
- Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes
Authors: Concepción Almoguera, Darryl Shibata, Kathleen Forrester, John J. Martin, Norman Arnheim, Manuel Perucho - Cell 1988 cited by 2,115
- Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B
Authors: Soo‐Kyung Choi, Song‐Ro Yoon, Peter Calabrese, Norman Arnheim - PLoS Genetics 2012 cited by 75
- Whole genome amplification from a single cell: implications for genetic analysis.
Authors: Lin Zhang, Xiufang Cui, Karin Schmitt, R Hubert, William Navidi, Norman Arnheim - National Academy of Sciences, Proceedings of the National Academy of Sciences 1992 cited by 902
- Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm
Authors: Andrew J. Wyrobek, Brenda Eskenazi, Suzanne Young, Norman Arnheim, Irene Tiemann‐Boege, Ethylin Wang Jabs, Rivka L. Glaser, Francesca Pearson, D.P. Evenson - National Academy of Sciences, Proceedings of the National Academy of Sciences 2006 cited by 398
- Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DMA mismatch repair
Authors: Tomas A. Prolla, Sean M. Baker, Allie C. Harris, Jen‐Lan Tsao, Xiang Yao, Christian Bronner, Binhai Zheng, Melissa D. Gordon, Jeffrey Reneker, Norman Arnheim, Darryl Shibata, Allan Bradley, R. Michael Liskay - Nature Genetics 1998 cited by 364
- A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues.
Authors: Gino Cortopassi, Darryl Shibata, Nay-Wei Soong, Norman Arnheim - National Academy of Sciences, Proceedings of the National Academy of Sciences 1992 cited by 640
- Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
Authors: Nay Wei Soong, David R. Hinton, Gino Cortopassi, Norman Arnheim - Nature Genetics 1992 cited by 419
- Understanding what determines the frequency and pattern of human germline mutations
Authors: Norman Arnheim, Peter Calabrese - Nature Reviews Genetics 2009 cited by 140
- Polyglutamine-Expanded Human Huntingtin Transgenes Induce Degeneration of Drosophila Photoreceptor Neurons
Authors: George R. Jackson, Iris Salecker, Xinzhong Dong, Xiang Yao, Norman Arnheim, Peter W. Faber, Marcy E. MacDonald, S Lawrence Zipursky - Neuron 1998 cited by 529
- Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
Authors: Sean M. Baker, Christian Bronner, Lin Zhang, Annemieke W. Plug, Merrilee Robatzek, Gwynedd Warren, Eileen A Elliott, Jian Yu, Terry Ashley, Norman Arnheim, Richard A. Flavell, R. Michael Liskay - Cell 1995 cited by 534
- Deleterious mitochondrial DNA mutations accumulate in aging human tissues
Authors: Norman Arnheim, Gino Cortopassi - Mutation Research/DNAging 1992 cited by 216
- The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect
Authors: Irene Tiemann‐Boege, William Navidi, Raji P. Grewal, D.H. Cohn, Brenda Eskenazi, Andrew J. Wyrobek, Norman Arnheim - National Academy of Sciences, Proceedings of the National Academy of Sciences 2002 cited by 166
- Contributions by MutL Homologues Mlh3 and Pms2 to DNA Mismatch Repair and Tumor Suppression in the Mouse
Authors: Peng‐Chieh Chen, Sandra Dudley, Wayne Hagen, Diana Dizon, Leslie Paxton, Denise Reichow, Song‐Ro Yoon, Kan Yang, Norman Arnheim, R. Michael Liskay, Steven M. Lipkin - Cancer Research 2005 cited by 97
- A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations
Authors: Soo‐Kyung Choi, Song‐Ro Yoon, Peter Calabrese, Norman Arnheim - National Academy of Sciences, Proceedings of the National Academy of Sciences 2008 cited by 91
- The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes
Authors: Jian Qin, Peter Calabrese, Irene Tiemann‐Boege, Deepali N. Shinde, Song‐Ro Yoon, David H. Gelfand, Keith Bauer, Norman Arnheim - PLoS Biology 2007 cited by 76
- Extension of base mispairs byTaqDNA polymerase: implications for single nucleotide discrimination in PCR
Authors: Mei-Mei Huang, Norman Arnheim, Myron F. Goodman - Nucleic Acids Research 1992 cited by 370
- Differential Contributions of Mammalian Rad54 Paralogs to Recombination, DNA Damage Repair, and Meiosis
Authors: Joanna Wesoły, Sheba Agarwal, Stefán Sigurðsson, Wendy Bussen, Stephen Van Komen, Jian Qin, Harry van Steeg, Jan van Benthem, Evelyne Wassenaar, Willy M. Baarends, Mehrnaz Ghazvini, Agnieszka A. Tafel, Helen Heath, Niels Galjart, Jeroen Essers, J. Anton Grootegoed, Norman Arnheim, Olga Bezzubova, Jean-Marie Buerstedde, Patrick Sung, Roland Kanaar - Molecular and Cellular Biology 2006 cited by 158
- Nup50, a Nucleoplasmically Oriented Nucleoporin with a Role in Nuclear Protein Export
Authors: Tinglu Guan, Ralph H. Kehlenbach, Eric C. Schirmer, Angelika Kehlenbach, Fan Fan, Bruce E. Clurman, Norman Arnheim, Larry Gerace - Molecular and Cellular Biology 2000 cited by 141
- Different mutator phenotypes in Mlh1 - versus Pms2 -deficient mice
Authors: Xiang Yao, Andrew B. Buermeyer, Latha Narayanan, Doan Duy Hai Tran, Sean M. Baker, Tomas A. Prolla, Peter M. Glazer, R. Michael Liskay, Norman Arnheim - National Academy of Sciences, Proceedings of the National Academy of Sciences 1999 cited by 137
- Huntington disease expansion mutations in humans can occur before meiosis is completed
Authors: Song‐Ro Yoon, Louis Dubeau, Margot de Young, Nancy S. Wexler, Norman Arnheim - National Academy of Sciences, Proceedings of the National Academy of Sciences 2003 cited by 104
