Chris Gunter

7.5k total citations · 1 hit paper
41 papers, 876 citations indexed

About

Chris Gunter is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Chris Gunter has authored 41 papers receiving a total of 876 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 17 papers in Molecular Biology and 9 papers in Cognitive Neuroscience. Recurrent topics in Chris Gunter's work include Autism Spectrum Disorder Research (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (5 papers). Chris Gunter is often cited by papers focused on Autism Spectrum Disorder Research (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (5 papers). Chris Gunter collaborates with scholars based in United States, United Kingdom and Belgium. Chris Gunter's co-authors include Marquitta J. White, Sam S. Oh, Ruth M. Greenblatt, Neil R. Powe, Esteban G. Burchard, Maria Pino‐Yanes, Kirsten Bibbins‐Domingo, Neeta Thakur, Luisa N. Borrell and Alan H.B. Wu and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature reviews. Cancer.

In The Last Decade

Chris Gunter

33 papers receiving 842 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diversity in Clinical and Biomedical Research: A Promise Yet to Be Fulfilled

2015 418 citations Sam S. Oh, Joshua Galanter et al. PLoS Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chris Gunter United States	11	304	276	203	124	121	41	876
Dena S. Davis United States	14	139 0.5×	92 0.3×	250 1.2×	67 0.5×	122 1.0×	91	745
R. Alta Charo United States	15	111 0.4×	480 1.7×	262 1.3×	131 1.1×	144 1.2×	58	1.0k
Josephine Johnston United States	16	137 0.5×	212 0.8×	149 0.7×	135 1.1×	46 0.4×	56	807
Erin Turbitt Australia	15	508 1.7×	125 0.5×	221 1.1×	81 0.7×	133 1.1×	87	901
Thomas H. Murray United States	19	255 0.8×	104 0.4×	355 1.7×	79 0.6×	262 2.2×	122	1.2k
Rachael E. Bennett United States	12	335 1.1×	213 0.8×	104 0.5×	175 1.4×	82 0.7×	14	587
Debra Mathews United States	16	178 0.6×	467 1.7×	253 1.2×	165 1.3×	101 0.8×	62	1.1k
Michelle N. Strecker United States	8	545 1.8×	119 0.4×	170 0.8×	63 0.5×	84 0.7×	10	1.1k
Jacalyn Duffin Canada	14	99 0.3×	79 0.3×	96 0.5×	194 1.6×	68 0.6×	84	878
Sarah S. Richardson United States	15	172 0.6×	76 0.3×	318 1.6×	48 0.4×	85 0.7×	44	870

Countries citing papers authored by Chris Gunter

Since Specialization

Citations

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

Fields of papers citing papers by Chris Gunter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chris Gunter. 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 Chris Gunter. The network helps show where Chris Gunter may publish in the future.

Co-authorship network of co-authors of Chris Gunter

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Wang, Amy, et al.. (2024). Provider-reported experiences, barriers, and perspectives on genetic testing as part of autism diagnosis. PLoS ONE. 19(2). e0296942–e0296942. 2 indexed citations

2.

Koehly, Laura M., et al.. (2022). Understanding changes in genetic literacy over time and in genetic research participants. The American Journal of Human Genetics. 109(12). 2141–2151. 15 indexed citations

3.

Gunter, Chris, et al.. (2021). Mini-Review: Genetic Literacy and Engagement With Genetic Testing for Autism Spectrum Disorder. Frontiers in Genetics. 12. 693158–693158. 1 indexed citations

4.

Raper, Jessica, et al.. (2021). Validation of the Social Responsiveness Scale (SRS) to screen for atypical social behaviors in juvenile macaques. PLoS ONE. 16(5). e0235946–e0235946. 11 indexed citations

5.

Telis, Natalie, et al.. (2019). Public Discussion Affects Question Asking at Academic Conferences. The American Journal of Human Genetics. 105(1). 189–197. 14 indexed citations

6.

Oh, Sam S., Joshua Galanter, Neeta Thakur, et al.. (2015). Diversity in Clinical and Biomedical Research: A Promise Yet to Be Fulfilled. PLoS Medicine. 12(12). e1001918–e1001918. 418 indexed citations breakdown →

7.

Gunter, Chris. (2012). Constructing a 'cancerpaedia'. Nature Reviews Drug Discovery. 11(5). 353–353.

8.

Gunter, Chris. (2012). Constructing a 'cancerpaedia'. Nature Reviews Genetics. 13(5). 300–300. 1 indexed citations

9.

Gunter, Chris. (2010). Get in LINE for silencing. Nature Reviews Genetics. 11(8). 528–529. 2 indexed citations

10.

Gunter, Chris. (2010). A picture worth 1000 Genomes. Nature Reviews Genetics. 11(12). 814–814. 7 indexed citations

11.

Gunter, Chris. (2009). A metamorphosis in synthesis. Nature Reviews Genetics. 11(1). 5–5. 3 indexed citations

12.

Lamb, Neil E., R Myers, & Chris Gunter. (2009). Education and Personalized Genomics: Deciphering the Public‘s Genetic Health Report. Personalized Medicine. 6(6). 681–690. 4 indexed citations

13.

DeWitt, Natalie, et al.. (2007). Epigenetics. Nature. 447(7143). 395–395. 45 indexed citations

14.

Gunter, Chris. (2006). The human touch. Nature reviews. Cancer. 6(S1). S21–S21.

15.

Gunter, Chris. (2002). Mosquitoes bite back on parasite transmission. Nature Reviews Genetics. 3(7). 497–497.

16.

Gunter, Chris. (2002). Turning up the heat on QTL mapping. Nature Reviews Genetics. 3(4). 237–237. 9 indexed citations

17.

Crawford, Dana C., Charles E. Schwartz, Kellen L. Meadows, et al.. (2000). Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population. The American Journal of Human Genetics. 66(2). 480–493. 44 indexed citations

18.

Holden, Jeanette J. A., Maire E. Percy, Diane Allingham‐Hawkins, et al.. (1999). Eighth International Workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997. American Journal of Medical Genetics. 83(4). 221–236. 3 indexed citations

19.

Gunter, Chris, William Paradee, Dana C. Crawford, et al.. (1998). Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Human Molecular Genetics. 7(12). 1935–1946. 59 indexed citations

20.

Brown, Victoria, Kersten M. Small, Yue Feng, et al.. (1998). Purified Recombinant Fmrp Exhibits Selective RNA Binding as an Intrinsic Property of the Fragile X Mental Retardation Protein. Journal of Biological Chemistry. 273(25). 15521–15527. 144 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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