K. Nichol

1.2k total citations
14 papers, 1.0k citations indexed

About

K. Nichol is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Atomic and Molecular Physics, and Optics. According to data from OpenAlex, K. Nichol has authored 14 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 2 papers in Atomic and Molecular Physics, and Optics. Recurrent topics in K. Nichol's work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and DNA Repair Mechanisms (4 papers). K. Nichol is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and DNA Repair Mechanisms (4 papers). K. Nichol collaborates with scholars based in Canada, United States and Japan. K. Nichol's co-authors include Christopher E. Pearson, Michael R. Hayden, Y. Paul Goldberg, Yuh‐Hwa Wang, John D. Cleary, Ichiro Kanazawa, Martina Metzler, Krista McCutcheon, Rona K. Graham and E. Almqvist and has published in prestigious journals such as Nature Genetics, Genome Research and Journal of Neurochemistry.

In The Last Decade

K. Nichol

14 papers receiving 992 citations

Peers

Countries citing papers authored by K. Nichol

Since Specialization

Citations

This map shows the geographic impact of K. Nichol's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by K. Nichol with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Nichol more than expected).

Fields of papers citing papers by K. Nichol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by K. Nichol. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by K. Nichol. The network helps show where K. Nichol may publish in the future.

Co-authorship network of co-authors of K. Nichol

This figure shows the co-authorship network connecting the top 25 collaborators of K. Nichol. A scholar is included among the top collaborators of K. Nichol based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with K. Nichol. K. Nichol is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	-NMR in thin metal films 2003 ·Physica B Condensed Matter ·W. A. MacFarlane, G. D. Morris, (unknown), K. H. Chow, R. Baartman, S. Daviel, S. R. Dunsiger, A. Hatakeyama, S. R. Kreitzman, C.D.P. Levy, R. I. Miller, K. Nichol, R. Poutissou, R. F. Kiefl	14
2	Quadrupolar split -NMR in SrTiO3 2003 ·Physica B Condensed Matter ·W. A. MacFarlane, G.D. Morris, K. H. Chow, R. Baartman, S. Daviel, S. R. Dunsiger, A. Hatakeyama, S. R. Kreitzman, C. D. P. Levy, R. I. Miller, K. Nichol, R. Poutissou, (unknown), L. H. Greene, R. F. Kiefl	22
3	Range straggling of low energy in thin metallic films using β-NMR 2003 ·Physica B Condensed Matter ·(unknown), R. F. Kiefl, W. A. MacFarlane, K. Nichol, G. D. Morris, C. D. P. Levy, S. R. Kreitzman, R. Poutissou, S. Daviel, R. Baartman, K. H. Chow	8
4	CpG Methylation Modifies the Genetic Stability of Cloned Repeat Sequences 2002 ·Genome Research ·K. Nichol, Christopher E. Pearson	46
5	Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells 2002 ·Nature Genetics ·John D. Cleary, K. Nichol, Yuh‐Hwa Wang, Christopher E. Pearson	158
6	Life Without Huntingtin 1999 ·Journal of Neurochemistry ·Martina Metzler, Nansheng Chen, Cheryl D. Helgason, Rona K. Graham, K. Nichol, Krista McCutcheon, Jamal Nasir, R. Keith Humphries, Lynn A. Raymond, Michael R. Hayden	33
7	A Yeast Artificial Chromosome-Based Physical Map of the Juvenile Amyotrophic Lateral Sclerosis (ALS2) Critical Region on Human Chromosome 2q33–q34 1999 ·Genomics ·(unknown), K. Nichol, Ryan R. Brinkman, Jamal Nasir, Duane W. Martindale, Ben F. Koop, Donald W. Nicholson, Stephen W. Scherer, Joh-E Ikeda, Michael R. Hayden	18
8	Genomic organization of the human caspase-9 gene on Chromosome 1p36.1-p36.3 1999 ·Mammalian Genome ·Jamal Nasir, K. Nichol, Dita Rasper, John P. Vaillancourt, (unknown), Barbara Beatty, Joh-E Ikeda, Michael R. Hayden	13
9	Gene structure and map location of the murine homolog of the Huntington-associated protein, Hap1 1998 ·Mammalian Genome ·Jamal Nasir, Kui Duan, K. Nichol, Simone Engelender, Roxann Ashworth, Veronica Colomer, (unknown), Christine M. Distèche, Michael R. Hayden	21
10	HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain 1997 ·Nature Genetics ·Michael A. Kalchman, Hiroshi Koide, Krista McCutcheon, Rona K. Graham, K. Nichol, Kazutoshi Nishiyama, Parsa Kazemi‐Esfarjani, Francis C. Lynn, Cheryl L. Wellington, Martina Metzler, Y. Paul Goldberg, Ichiro Kanazawa, R D Gietz, Michael R. Hayden	313
11	Contribution of DNA Sequence and CAG Size to Mutation Frequencies of Intermediate Alleles for Huntington Disease: Evidence from Single Sperm Analyses 1997 ·Human Molecular Genetics ·Samuel S. Chong, E. Almqvist, H. Telenius, (unknown), K. Nichol, (unknown), Y. Paul Goldberg, Bassem R. Haddad, Fiona Richards, David Sillence, Cheryl R. Greenberg, Elizabeth Ives, Ger van den Engh, Mark Hughes, Michael R. Hayden	92
12	Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease 1995 ·Human Molecular Genetics ·E. Almqvist, Niamh Spence, K. Nichol, Susan E. Andrew, J. Vesa, Leena Peltonen, Maria Anvret, Jun Goto, Ichiro Kanazawa, Y. Paul Goldberg, Michael R. Hayden	59
13	Somatic mosaicism in sperm is associated with intergenerational (CAG)_n changes in Huntington disease 1995 ·Human Molecular Genetics ·H. Telenius, E. Almqvist, B Kremer, Niamh Spence, Ferdinando Squitieri, K. Nichol, Ulla Grandell, (unknown), Caroline Benjamin, Imma Castaldo, Olga Calabrese, Maria Anvret, Y. Paul Goldberg, Michael R. Hayden	67
14	DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence 1994 ·Human Molecular Genetics ·Ferdinando Squitieri, Susan E. Andrew, Y. Paul Goldberg, B Kremer, Niamh Spence, (unknown), K. Nichol, Jane Theilmann, Jacquie Greenberg, Jun Goto, Ichiro Kanazawa, J. Vesa, Leena Peltonen, E. Almqvist, Maria Anvret, H. Telenius, Binshan Lin, G. Napolitano, Kenneth Morgan, Michael R. Hayden	148

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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