Stephen G. Kahler

6.6k total citations
84 papers, 4.1k citations indexed

About

Stephen G. Kahler is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Stephen G. Kahler has authored 84 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 30 papers in Clinical Biochemistry and 26 papers in Genetics. Recurrent topics in Stephen G. Kahler's work include Metabolism and Genetic Disorders (30 papers), Mitochondrial Function and Pathology (14 papers) and Autism Spectrum Disorder Research (12 papers). Stephen G. Kahler is often cited by papers focused on Metabolism and Genetic Disorders (30 papers), Mitochondrial Function and Pathology (14 papers) and Autism Spectrum Disorder Research (12 papers). Stephen G. Kahler collaborates with scholars based in United States, Australia and Canada. Stephen G. Kahler's co-authors include David S. Millington, Charles R. Roe, Donald H. Chace, Shannon Rose, Richard E. Frye, Naoto Terada, Steven L Hillman, L F Hofman, Marie Tippett and James L. Wilkinson and has published in prestigious journals such as New England Journal of Medicine, JAMA and Journal of Biological Chemistry.

In The Last Decade

Stephen G. Kahler

84 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen G. Kahler United States 33 1.9k 1.5k 870 592 571 84 4.1k
Russell P. Saneto United States 31 2.3k 1.2× 1.2k 0.9× 417 0.5× 228 0.4× 575 1.0× 112 4.1k
Rafael Artuch Spain 45 3.7k 1.9× 2.5k 1.7× 853 1.0× 256 0.4× 562 1.0× 291 6.9k
Sídney M. Gospe United States 30 896 0.5× 969 0.7× 228 0.3× 99 0.2× 676 1.2× 96 2.8k
Rosario Rich Trifiletti United States 25 1.1k 0.6× 410 0.3× 244 0.3× 147 0.2× 229 0.4× 68 3.4k
Laura Mazzanti Italy 36 1.6k 0.8× 206 0.1× 1.3k 1.5× 105 0.2× 445 0.8× 250 4.5k
Salvatore Grosso Italy 36 1.4k 0.7× 277 0.2× 1.0k 1.2× 243 0.4× 1.1k 1.9× 152 4.3k
Francesco Mari Italy 39 1.8k 1.0× 94 0.1× 393 0.5× 469 0.8× 205 0.4× 162 4.0k
Lars Hagenfeldt Sweden 42 1.8k 0.9× 1.3k 0.9× 336 0.4× 41 0.1× 291 0.5× 165 6.1k
Richard G. Boles United States 32 1.1k 0.6× 831 0.6× 261 0.3× 61 0.1× 251 0.4× 75 2.7k
Rita Christopher India 28 699 0.4× 226 0.2× 177 0.2× 245 0.4× 156 0.3× 181 2.9k

Countries citing papers authored by Stephen G. Kahler

Since Specialization
Citations

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

Fields of papers citing papers by Stephen G. Kahler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen G. Kahler. 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 Stephen G. Kahler. The network helps show where Stephen G. Kahler may publish in the future.

Co-authorship network of co-authors of Stephen G. Kahler

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

All Works

20 of 20 papers shown
1.
Harville, Terry, Sirish C. Bennuri, Leanna Delhey, et al.. (2019). Inheritance of HLA-Cw7 Associated With Autism Spectrum Disorder (ASD). Frontiers in Psychiatry. 10. 612–612. 15 indexed citations
2.
Rose, Shannon, Sirish C. Bennuri, Rebecca Wynne, et al.. (2018). Butyrate enhances mitochondrial function during oxidative stress in cell lines from boys with autism. Translational Psychiatry. 8(1). 42–42. 159 indexed citations
3.
Frye, Richard E., Shannon Rose, Joseph G. Chacko, et al.. (2016). Modulation of mitochondrial function by the microbiome metabolite propionic acid in autism and control cell lines. Translational Psychiatry. 6(10). e927–e927. 100 indexed citations
4.
Frye, Richard E., Leanna Delhey, John M. Slattery, et al.. (2016). Blocking and Binding Folate Receptor Alpha Autoantibodies Identify Novel Autism Spectrum Disorder Subgroups. Frontiers in Neuroscience. 10. 80–80. 55 indexed citations
5.
Sanmann, Jennifer N., Lois J. Starr, Diane L. Pickering, et al.. (2012). Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome. American Journal of Medical Genetics Part A. 158A(6). 1285–1291. 19 indexed citations
6.
Ware, Stephanie M., Nahed O. ElHassan, Stephen G. Kahler, et al.. (2009). Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes. Journal of Medical Genetics. 46(5). 308–314. 70 indexed citations
7.
Stamm, Demetra S., Cynthia M. Powell, Jeffrey M. Stajich, et al.. (2008). Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1. Neurology. 71(22). 1764–1769. 23 indexed citations
8.
Stamm, Demetra S., Arthur S. Aylsworth, Jeffrey M. Stajich, et al.. (2008). Native American myopathy: Congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia. American Journal of Medical Genetics Part A. 146A(14). 1832–1841. 50 indexed citations
9.
Herbert, Martha R., John Russo, San‐Duk Yang, et al.. (2006). Autism and environmental genomics. NeuroToxicology. 27(5). 671–684. 124 indexed citations
10.
Smith, Wendy E., Stephen G. Kahler, Donald P. Frush, et al.. (2001). Hepatic storage of glycogen in Niemann-Pick disease type B. The Journal of Pediatrics. 138(6). 946–948. 2 indexed citations
11.
Wang, Menglin, et al.. (1996). Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.. Journal of Medical Genetics. 33(9). 760–763. 19 indexed citations
12.
Hove, Johan L.K. Van, Gail A. Spiridigliozzi, R Heinz, et al.. (1995). Fryns syndrome survivors and neurologic outcome. American Journal of Medical Genetics. 59(3). 334–340. 29 indexed citations
13.
Hove, Johan L.K. Van, S. Lane Rutledge, Mohamed A. Nada, Stephen G. Kahler, & David S. Millington. (1994). 3‐Hydroxyisovalerylcarnitine in 3‐methylcrotonyl‐CoA carboxylase deficiency. Journal of Inherited Metabolic Disease. 18(5). 592–601. 26 indexed citations
14.
Hove, Johan L.K. Van, Sara Shanske, Scott W. Ballinger, et al.. (1994). Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: A distinct late onset mitochondrial disorder. American Journal of Medical Genetics. 51(2). 114–120. 5 indexed citations
15.
Kahler, Stephen G., David S. Millington, Diane S. Roe, et al.. (1994). Intravenous L-Carnitine and Acetyl-L-Carnitine in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency and Isovaleric Acidemia. Pediatric Research. 35(1). 96–101. 16 indexed citations
16.
Lubinsky, Mark, et al.. (1994). von Voss‐Cherstvoy syndrome: A variable perinatally lethal syndrome of multiple congenital anomalies. American Journal of Medical Genetics. 52(3). 272–278. 12 indexed citations
17.
Hove, Johan L.K. Van, et al.. (1992). Unbalanced translocation 46,xy,−15,+der(22)t(15;22)(q13;q11)pat: Case report and review of the literature. American Journal of Medical Genetics. 44(1). 24–30. 7 indexed citations
18.
McConkie‐Rosell, Allyn, Yuan‐Tsong Chen, David J. Harris, et al.. (1989). Mild Cystic Fibrosis Linked to Chromosome 7q22 Markers with an Uncommon Haplotype. Annals of Internal Medicine. 111(10). 797–801. 6 indexed citations
19.
Knowles, Michael, et al.. (1989). Mild Cystic Fibrosis in a Consanguineous Family. Annals of Internal Medicine. 110(8). 599–605. 13 indexed citations
20.
Stewart, Charles R., Stephen G. Kahler, & James M. Gilchrist. (1988). Congenital myopathy with cleft palate and increased susceptibility to malignant hyperthermia: King syndrome?. Pediatric Neurology. 4(6). 371–374. 14 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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