Kristin Herman

1.0k total citations
12 papers, 599 citations indexed

About

Kristin Herman is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Kristin Herman has authored 12 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Neurology. Recurrent topics in Kristin Herman's work include Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (2 papers) and Congenital heart defects research (2 papers). Kristin Herman is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (2 papers) and Congenital heart defects research (2 papers). Kristin Herman collaborates with scholars based in United States, Israel and United Kingdom. Kristin Herman's co-authors include Randi J. Hagerman, Jessica Ferranti, Flora Tassone, David Hessl, Susan Harris, Susan Bacalman, Ingrid Tremel Barbato, Beth L. Goodlin‐Jones, Paul J. Hagerman and Kara E. Koehler and has published in prestigious journals such as Nature Genetics, Neurology and The American Journal of Human Genetics.

In The Last Decade

Kristin Herman

12 papers receiving 586 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kristin Herman United States 7 371 270 266 69 63 12 599
Ravinesh A. Kumar United States 10 508 1.4× 364 1.3× 278 1.0× 43 0.6× 83 1.3× 16 767
Ismail Thanseem Japan 15 317 0.9× 462 1.7× 262 1.0× 47 0.7× 98 1.6× 28 877
James Jaworski United States 17 588 1.6× 372 1.4× 546 2.1× 32 0.5× 153 2.4× 19 951
Tiffany Vu United States 8 469 1.3× 341 1.3× 191 0.7× 63 0.9× 35 0.6× 9 691
Meredyth P. Bass United States 14 779 2.1× 350 1.3× 475 1.8× 40 0.6× 73 1.2× 17 1.1k
Markéta Havlovičová Czechia 14 274 0.7× 244 0.9× 215 0.8× 21 0.3× 135 2.1× 33 643
John B. Vincent Canada 11 878 2.4× 656 2.4× 539 2.0× 54 0.8× 113 1.8× 19 1.1k
Elena Bacchelli Italy 16 512 1.4× 343 1.3× 383 1.4× 23 0.3× 96 1.5× 28 791
Alexis Rea United States 6 321 0.9× 218 0.8× 279 1.0× 19 0.3× 73 1.2× 7 619
Angelika Rieß Germany 11 460 1.2× 411 1.5× 245 0.9× 17 0.2× 98 1.6× 20 756

Countries citing papers authored by Kristin Herman

Since Specialization
Citations

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

Fields of papers citing papers by Kristin Herman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristin Herman

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

All Works

12 of 12 papers shown
1.
Jiang, Shiyan, et al.. (2025). Analysing nontraditional students' ChatGPT interaction, engagement, self‐efficacy and performance: A mixed‐methods approach. British Journal of Educational Technology. 56(5). 1973–2000. 2 indexed citations
2.
Smith, Thomas B., Huw B. Thomas, Kyle Thompson, et al.. (2023). Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54. European Journal of Human Genetics. 31(10). 1190–1194. 3 indexed citations
3.
Herman, Kristin, et al.. (2022). Past Precedent. 2 indexed citations
4.
Prange, Lyndsey, Kristin Herman, Raphael Schiffmann, et al.. (2020). D-DEMØ, a distinct phenotype caused by ATP1A3 mutations. Neurology Genetics. 6(5). e466–e466. 20 indexed citations
5.
Prange, Lyndsey, Vandana Shashi, Kristin Herman, et al.. (2017). D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations (P4.157). Neurology. 88(16_supplement). 1 indexed citations
6.
Fernández‐Guerra, Paula, Rune Isak Dupont Birkler, Shahar Nisemblat, et al.. (2016). Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental Disorder. Frontiers in Molecular Biosciences. 3. 65–65. 37 indexed citations
7.
Lozano, Reymundo, Kristin Herman, Pınar Bayrak‐Toydemir, et al.. (2016). Clinical intrafamilial variability in lethal familial neonatal seizure disorder caused by TBC1D24 mutations. American Journal of Medical Genetics Part A. 170(12). 3207–3214. 17 indexed citations
8.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Carolyn Bay, et al.. (2011). Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44. European Journal of Human Genetics. 20(2). 176–179. 38 indexed citations
9.
Harris, Susan, David Hessl, Beth L. Goodlin‐Jones, et al.. (2008). Autism Profiles of Males With Fragile X Syndrome. American Journal on Mental Retardation. 113(6). 427–438. 303 indexed citations
10.
Kovach, Margaret J., et al.. (2000). Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families. Genetics in Medicine. 2(5). 283–289. 4 indexed citations
11.
Kovach, Margaret J., Jing‐Ping Lin, Simeon A. Boyadjiev, et al.. (1999). A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness. The American Journal of Human Genetics. 64(6). 1580–1593. 56 indexed citations
12.
Koehler, Kara E., Christina Boulton, Rachael L. French, et al.. (1996). Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories. Nature Genetics. 14(4). 406–414. 116 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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