Mark W. Neff

1.9k total citations
19 papers, 1.3k citations indexed

About

Mark W. Neff is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Mark W. Neff has authored 19 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Cell Biology. Recurrent topics in Mark W. Neff's work include Human-Animal Interaction Studies (5 papers), Genomics and Phylogenetic Studies (4 papers) and Microtubule and mitosis dynamics (3 papers). Mark W. Neff is often cited by papers focused on Human-Animal Interaction Studies (5 papers), Genomics and Phylogenetic Studies (4 papers) and Microtubule and mitosis dynamics (3 papers). Mark W. Neff collaborates with scholars based in United States, Canada and Finland. Mark W. Neff's co-authors include Aaron K. Wong, Alison L. Ruhe, Karl W. Broman, Daniel J. Burke, Jasper Rine, Kathryn Robertson, Elaine A. Ostrander, Joshua M. Akey, Jennifer Madeoy and Caitlin Connelly and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Mark W. Neff

19 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mark W. Neff United States 15 714 480 157 143 112 19 1.3k
Darla R. Miller United States 23 804 1.1× 949 2.0× 71 0.5× 192 1.3× 74 0.7× 61 2.3k
E. Gootwine Israel 27 1.2k 1.6× 565 1.2× 70 0.4× 62 0.4× 69 0.6× 92 2.1k
Nobumoto Miyashita Japan 19 678 0.9× 632 1.3× 96 0.6× 205 1.4× 96 0.9× 46 1.3k
Daniel Nilsson Sweden 28 368 0.5× 1.2k 2.6× 103 0.7× 128 0.9× 60 0.5× 87 2.2k
Carole A. Sargent United Kingdom 28 1.1k 1.6× 1.2k 2.6× 101 0.6× 48 0.3× 89 0.8× 71 2.5k
Junfeng Pang China 22 523 0.7× 583 1.2× 282 1.8× 227 1.6× 79 0.7× 42 1.5k
Gerli Pielberg Sweden 17 794 1.1× 485 1.0× 244 1.6× 48 0.3× 33 0.3× 25 1.3k
Alex Van Zeveren Belgium 22 712 1.0× 810 1.7× 72 0.5× 53 0.4× 30 0.3× 92 1.8k
Robert A. Grahn United States 24 630 0.9× 575 1.2× 254 1.6× 91 0.6× 18 0.2× 69 1.5k
Marcia M. Miller United States 30 455 0.6× 763 1.6× 66 0.4× 99 0.7× 66 0.6× 74 2.7k

Countries citing papers authored by Mark W. Neff

Since Specialization
Citations

This map shows the geographic impact of Mark W. Neff'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 Mark W. Neff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark W. Neff more than expected).

Fields of papers citing papers by Mark W. Neff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark W. Neff. 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 Mark W. Neff. The network helps show where Mark W. Neff may publish in the future.

Co-authorship network of co-authors of Mark W. Neff

This figure shows the co-authorship network connecting the top 25 collaborators of Mark W. Neff. A scholar is included among the top collaborators of Mark W. Neff 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 Mark W. Neff. Mark W. Neff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Webb, Aubrey A., Alison L. Ruhe, & Mark W. Neff. (2019). A missense mutation in MYO7A is associated with bilateral deafness and vestibular dysfunction in the Doberman pinscher breed.. PubMed. 83(2). 142–148. 9 indexed citations
2.
Paoloni, Melissa, Craig P. Webb, Christina Mazcko, et al.. (2014). Prospective Molecular Profiling of Canine Cancers Provides a Clinically Relevant Comparative Model for Evaluating Personalized Medicine (PMed) Trials. PLoS ONE. 9(3). e90028–e90028. 26 indexed citations
3.
Wong, Aaron K., Alison L. Ruhe, Shameek Biswas, et al.. (2012). Marker Panels for Genealogy-Based Mapping, Breed Demographics, and Inference-of-Ancestry in the Dog. Animal Biotechnology. 23(4). 241–252. 1 indexed citations
4.
Yokoyama, Jennifer S., Ernest T. Lam, Alison L. Ruhe, et al.. (2012). Variation in Genes Related to Cochlear Biology Is Strongly Associated with Adult-Onset Deafness in Border Collies. PLoS Genetics. 8(9). e1002898–e1002898. 19 indexed citations
5.
Neff, Mark W., John S. Beck, Julie Koeman, et al.. (2012). Partial Deletion of the Sulfate Transporter SLC13A1 Is Associated with an Osteochondrodysplasia in the Miniature Poodle Breed. PLoS ONE. 7(12). e51917–e51917. 21 indexed citations
6.
Wong, Aaron K., Alison L. Ruhe, Kathryn Robertson, et al.. (2012). Ade novomutation inKITcauses white spotting in a subpopulation ofGermanShepherd dogs. Animal Genetics. 44(3). 305–310. 30 indexed citations
7.
Greer, Kimberly A., Aaron K. Wong, Thomas R. Famula, et al.. (2010). Necrotizing meningoencephalitis of Pug Dogs associates with dog leukocyte antigen class II and resembles acute variant forms of multiple sclerosis. Tissue Antigens. 76(2). 110–8. 69 indexed citations
8.
Bader, Hannah L., Alison L. Ruhe, Lauren W. Wang, et al.. (2010). An ADAMTSL2 Founder Mutation Causes Musladin-Lueke Syndrome, a Heritable Disorder of Beagle Dogs, Featuring Stiff Skin and Joint Contractures. PLoS ONE. 5(9). e12817–e12817. 34 indexed citations
9.
Akey, Joshua M., Alison L. Ruhe, Dayna T. Akey, et al.. (2010). Tracking footprints of artificial selection in the dog genome. Proceedings of the National Academy of Sciences. 107(3). 1160–1165. 247 indexed citations
10.
Cadieu, Édouard, Mark W. Neff, Pascale Quignon, et al.. (2009). Coat Variation in the Domestic Dog Is Governed by Variants in Three Genes. Science. 326(5949). 150–153. 244 indexed citations
11.
Wong, Aaron K. & Mark W. Neff. (2009). DOGSET: pre‐designed primer sets for fine‐scale mapping and DNA sequence interrogation in the dog. Animal Genetics. 40(4). 569–571. 10 indexed citations
12.
Wong, Aaron K., Alison L. Ruhe, Beth L. Dumont, et al.. (2009). A Comprehensive Linkage Map of the Dog Genome. Genetics. 184(2). 595–605. 79 indexed citations
13.
Neff, Mark W. & Jasper Rine. (2006). A Fetching Model Organism. Cell. 124(2). 229–231. 50 indexed citations
14.
Neff, Mark W., Kathryn Robertson, Aaron K. Wong, et al.. (2004). Breed distribution and history of canine mdr1-1Δ , a pharmacogenetic mutation that marks the emergence of breeds from the collie lineage. Proceedings of the National Academy of Sciences. 101(32). 11725–11730. 147 indexed citations
15.
Harding, Cary O., et al.. (2003). Expression of phenylalanine hydroxylase (PAH) in erythrogenic bone marrow does not correct hyperphenylalaninemia in Pahenu2 mice. The Journal of Gene Medicine. 5(11). 984–993. 10 indexed citations
16.
Neff, Mark W., Karl W. Broman, Cathryn S. Mellersh, et al.. (1999). A Second-Generation Genetic Linkage Map of the Domestic Dog, Canis familiaris. Genetics. 151(2). 803–820. 182 indexed citations
17.
Neff, Mark W. & Daniel J. Burke. (1992). A Delay in the Saccharomyces cerevisiae Cell Cycle That Is Induced by a Dicentric Chromosome and Dependent upon Mitotic Checkpoints. Molecular and Cellular Biology. 12(9). 3857–3864. 14 indexed citations
18.
Neff, Mark W. & Daniel J. Burke. (1992). A delay in the Saccharomyces cerevisiae cell cycle that is induced by a dicentric chromosome and dependent upon mitotic checkpoints.. Molecular and Cellular Biology. 12(9). 3857–3864. 41 indexed citations
19.
Neff, Mark W. & Daniel J. Burke. (1991). Random segregation of chromatids at mitosis in Saccharomyces cerevisiae.. Genetics. 127(3). 463–473. 34 indexed citations

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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