S. Lane Rutledge

2.5k total citations
31 papers, 1.3k citations indexed

About

S. Lane Rutledge is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, S. Lane Rutledge has authored 31 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in S. Lane Rutledge's work include Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (10 papers) and Genomic variations and chromosomal abnormalities (4 papers). S. Lane Rutledge is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (10 papers) and Genomic variations and chromosomal abnormalities (4 papers). S. Lane Rutledge collaborates with scholars based in United States, Canada and Switzerland. S. Lane Rutledge's co-authors include Huda Y. Zoghbi, Maria Descartes, Nathaniel H. Robin, Andrew J. Carroll, Tetsuo Ashizawa, Saeed Bohlega, Fady M. Mikhail, Morey W. Haymond, O. Colin Stine and Orest Hurko and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Neurology.

In The Last Decade

S. Lane Rutledge

31 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
S. Lane Rutledge United States 19 844 519 295 252 152 31 1.3k
Carl Fratter United Kingdom 26 945 1.1× 530 1.0× 141 0.5× 184 0.7× 48 0.3× 47 1.3k
Shoji Yano United States 17 386 0.5× 269 0.5× 107 0.4× 162 0.6× 87 0.6× 57 858
Parayil Sankaran Bindu India 19 386 0.5× 177 0.3× 192 0.7× 80 0.3× 166 1.1× 92 1.1k
I. E. M. Luyt‐Houwen Netherlands 14 866 1.0× 564 1.1× 83 0.3× 78 0.3× 54 0.4× 26 1.1k
Jörg Klepper Germany 20 555 0.7× 759 1.5× 132 0.4× 213 0.8× 145 1.0× 42 1.6k
Luísa Diogo Portugal 20 790 0.9× 622 1.2× 54 0.2× 304 1.2× 143 0.9× 71 1.4k
Lynne A. Wolfe United States 15 742 0.9× 297 0.6× 77 0.3× 264 1.0× 41 0.3× 49 1.1k
K Naess Sweden 15 740 0.9× 466 0.9× 76 0.3× 112 0.4× 41 0.3× 41 974
Donald T. Whelan Canada 20 488 0.6× 224 0.4× 97 0.3× 243 1.0× 166 1.1× 42 917
Yoshinobu Ohtani Japan 12 339 0.4× 275 0.5× 92 0.3× 111 0.4× 291 1.9× 25 726

Countries citing papers authored by S. Lane Rutledge

Since Specialization
Citations

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

Fields of papers citing papers by S. Lane Rutledge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Lane Rutledge. 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 S. Lane Rutledge. The network helps show where S. Lane Rutledge may publish in the future.

Co-authorship network of co-authors of S. Lane Rutledge

This figure shows the co-authorship network connecting the top 25 collaborators of S. Lane Rutledge. A scholar is included among the top collaborators of S. Lane Rutledge 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 S. Lane Rutledge. S. Lane Rutledge 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.
Larson, Austin, Shanti Balasubramaniam, John Christodoulou, et al.. (2018). Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6. Mitochondrion. 44. 58–64. 17 indexed citations
2.
Theunissen, Tom E. J., Radek Szklarczyk, Mike Gerards, et al.. (2016). Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects. Frontiers in Neurology. 7. 203–203. 21 indexed citations
3.
Rutledge, S. Lane, et al.. (2016). Fore-arc structure, plate coupling and isostasy in the Central Andes: Insight from gravity data modelling. Journal of Geodynamics. 104. 27–35. 2 indexed citations
4.
Schmidt, Wolfgang M., S. Lane Rutledge, Rebecca Schüle, et al.. (2015). Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia. The American Journal of Human Genetics. 97(6). 855–861. 39 indexed citations
5.
Mikhail, Fady M., Rachel D. Burnside, Jennifer Ibrahim, et al.. (2013). The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system. Genetics in Medicine. 16(1). 92–100. 34 indexed citations
6.
Mikhail, Fady M., Edward J. Lose, Nathaniel H. Robin, et al.. (2011). Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders. American Journal of Medical Genetics Part A. 155(10). 2386–2396. 129 indexed citations
7.
Dimmock, David, Lin-ya Tang, Maria Descartes, et al.. (2009). A novel c.592-4_c.592-3delTT mutation in DGUOK gene causes exon skipping. Mitochondrion. 10(2). 188–191. 13 indexed citations
8.
He, Miao, S. Lane Rutledge, David R. Kelly, et al.. (2007). A New Genetic Disorder in Mitochondrial Fatty Acid β-Oxidation: ACAD9 Deficiency. The American Journal of Human Genetics. 81(1). 87–103. 91 indexed citations
9.
Rutledge, S. Lane, et al.. (2007). Abnormal White Matter in a Neurologically Intact Child With Incontinentia Pigmenti. Pediatric Neurology. 36(3). 199–201. 12 indexed citations
10.
Tubbs, R. Shane, et al.. (2004). Chiari I malformation and neurofibromatosis type 1. Pediatric Neurology. 30(4). 278–280. 40 indexed citations
11.
Percy, Alan K. & S. Lane Rutledge. (2001). Adrenoleukodystrophy and related disorders. Mental Retardation and Developmental Disabilities Research Reviews. 7(3). 179–189. 8 indexed citations
12.
Wise, Merrill S., S. Lane Rutledge, & Ruben Kuzniecky. (1996). Rasmussen syndrome and long-term response to gamma globulin. Pediatric Neurology. 14(2). 149–152. 23 indexed citations
13.
Gouw, Launce, Craig D. Kaplan, Kathleen B. Digre, et al.. (1995). Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p. Nature Genetics. 10(1). 89–93. 110 indexed citations
14.
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
15.
Rutledge, S. Lane, et al.. (1993). Tubulointerstitial nephritis in methylmalonic acidemia. Pediatric Nephrology. 7(1). 81–82. 35 indexed citations
16.
Hurko, Orest, Donald R. Johns, S. Lane Rutledge, et al.. (1990). Heteroplasmy in Chronic External Ophthalmoplegia: Clinical and Molecular Observations. Pediatric Research. 28(5). 542–548. 18 indexed citations
17.
Rutledge, S. Lane, Peter L. Havens, Morey W. Haymond, et al.. (1990). Neonatal hemodialysis: Effective therapy for the encephalopathy of inborn errors of metabolism. The Journal of Pediatrics. 116(1). 125–128. 61 indexed citations
18.
Rutledge, S. Lane, et al.. (1989). Pyruvate carboxylase deficiency: Acute exacerbation after ACTH treatment of infantile spasms. Pediatric Neurology. 5(4). 249–252. 16 indexed citations
19.
Johns, D. R., S. Lane Rutledge, O. Colin Stine, & Orest Hurko. (1989). Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.. Proceedings of the National Academy of Sciences. 86(20). 8059–8062. 69 indexed citations
20.
Rutledge, S. Lane & O. Carter Snead. (1986). Neurologic complications of immunizations. The Journal of Pediatrics. 109(6). 917–924. 9 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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