Sara Shanske

16.4k citations

188 papers · 12.1k indexed · 2 hit papers · h-index 60

Molecular Biology top 0.5%
Clinical Biochemistry top 0.01%
Rheumatology top 0.5%
Cellular and Molecular Neuroscience top 1%
Genetics top 2%

Co-authors: S. DiMauro Salvatore DiMauro Eric A. Schon Carlos T. Moraes Eduardo Bonilla Michio Hirano Filippo M. Santorelli Seiichi Tsujino
Topics: Mitochondrial Function and Pathology (126 papers)Metabolism and Genetic Disorders (109 papers)ATP Synthase and ATPases Research (61 papers)
Cited by: Clinical Biochemistry Molecular Biology Rheumatology
Journals: Nature New England Journal of Medicine The Lancet
Partner nations: United States Italy Canada

In The Last Decade

Sara Shanske

188 papers receiving 11.7k 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.

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

1989 746 citations Carlos T. Moraes, Salvatore DiMauro et al. profile →
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

2000 702 citations Kurenai Tanji, Carolyn M. Sue et al. profile →

Peers

Countries citing papers authored by Sara Shanske

Since Specialization

Citations

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

Fields of papers citing papers by Sara Shanske

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Shanske

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNALeu(CUN) gene 2009 ·Journal of the Neurological Sciences ·Jorida Çoku,Sara Shanske,(unknown),Kurenai Tanji,Ali Naini,Valentina Emmanuele,Marc C. Patterson,Michio Hirano,Salvatore DiMauro	4
2	Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene 2008 ·Neuromuscular Disorders ·Belén Bornstein,Estela Área-Gómez,Kevin M. Flanigan,Jaya Ganesh,Parul Jayakar,Kathryn J. Swoboda,Jorida Çoku,Ali Naini,Sara Shanske,Kurenai Tanji,Michio Hirano,Salvatore DiMauro	65
3	Fatal Infantile Cardiac Glycogenosis with Phosphorylase Kinase Deficiency and a Mutation in the γ2-Subunit of AMP-Activated Protein Kinase 2007 ·Pediatric Research ·Hasan O. Akman,James N. Sampayo,Fiona A. Ross,John W. Scott,Gregory J. Wilson,Lee Benson,Claudio Bruno,Sara Shanske,D. Grahame Hardie,Salvatore DiMauro	41
4	Unusual Clinical Presentations in Four Cases of Leigh Disease, Cytochrome C Oxidase Deficiency, and SURF1 Gene Mutations 2005 ·Journal of Child Neurology ·S K Tay,Sabrina Sacconi,(unknown),(unknown),Augusto Morales,Darryl C. De Vivo,Sara Shanske,Eduardo Bonilla,Salvatore DiMauro	25
5	Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene 2003 ·Journal of the Neurological Sciences ·Michelangelo Mancuso,Massimiliano Filosto,J. Clarke Stevens,Marc C. Patterson,Sara Shanske,Sindu Krishna,Salvatore DiMauro	33
6	Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) gene 1999 ·Neuromuscular Disorders ·Georgios M. Hadjigeorgiou,Noriko Kawashima,Claudio Bruno,Antoni L. Andreu,Carolyn M. Sue,Daniel J. Rigden,(unknown),Sara Shanske,S. DiMauro	23
7	Infantile encephalopathy associated with the MELAS A3243G mutation 1999 ·The Journal of Pediatrics ·Carolyn M. Sue,Claudio Bruno,Antoni L. Andreu,(unknown),Jerry R. Mendell,Chang‐Yong Tsao,Mark Luquette,Juliann Paolicchi,Sara Shanske,Salvatore DiMauro,Darryl C. De Vivo	52
8	Genetic Counseling and Prenatal Diagnosis for the Mitochondrial DNA Mutations at Nucleotide 8993 1999 ·The American Journal of Human Genetics ·S. L. White,Veronica Collins,Rory Wolfe,Maureen Cleary,Sara Shanske,S. DiMauro,Hans‐Henrik M. Dahl,David R. Thorburn	157
9	Early Onset of Diabetes Mellitus Associated with the Mitochondrial DNA T14709C Point Mutation: Patient Report and Literature Review 1999 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown),Phyllis Speiser,Alfred E. Slonim,Maria I. New,Sara Shanske,Weibo Xia,Filippo M. Santorelli,S. DiMauro	27
10	Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindred 1996 ·Muscle & Nerve ·António Toscano,Seiichi Tsujino,Giuseppe Vita,Sara Shanske,C Messina,Salvatore DiMauro	29
11	Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's disease 1996 ·Neuromuscular Disorders ·(unknown),Sara Shanske,Stephanie J. Valberg,George H. Cardinet,Bradford P. Smith,S. DiMauro	29
12	High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathy 1995 ·Neurology ·Giovanni Manfredi,Serenella Servidei,E. Bonilla,Sara Shanske,Eric A. Schon,S. DiMauro,Carlos T. Moraes	27
13	A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis 1995 ·Annals of Neurology ·(unknown),Sara Shanske,(unknown),Darryl C. DeVivo,Salvatore DiMauro	136
14	Myophosphorylase deficiency associated with rhabdomyolysis and exercise intolerance in 6 related charolais cattle 1995 ·Muscle & Nerve ·(unknown),Stephanie J. Valberg,Bradford P. Smith,(unknown),Sara Shanske,Seiichi Tsujino,S. DiMauro,George H. Cardinet	37
15	The molecular genetic basis of myophosphorylase deficiency (McArdle's disease) 1995 ·Muscle & Nerve ·Seiichi Tsujino,Sara Shanske,Ikuya Nonaka,S. DiMauro	41
16	Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency 1995 ·Muscle & Nerve ·Seiichi Tsujino,Sara Shanske,Salvatore DiMauro	20
17	Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: A distinct late onset mitochondrial disorder 1994 ·American Journal of Medical Genetics ·Johan L.K. Van Hove,Sara Shanske,(unknown),Scott W. Ballinger,(unknown),Douglas C. Wallace,Takashi Hanioka,Karl Folkers,Edward H. Bossen,Peter S. Kussin,(unknown),Stephen G. Kahler	5
18	A new mtDNA mutation in the tRNALeu(UUR) gene associated with maternally inherited cardiomyopathy 1994 ·Human Mutation ·Gabriella Silvestri,Filippo M. Santorelli,Sara Shanske,C B Whitley,Lisa A. Schimmenti,Sabrina Smith,S. DiMauro	141
19	Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients 1994 ·Annals of Neurology ·Seiichi Tsujino,Sara Shanske,A. Keith W. Brownell,Ronald G. Haller,Salvatore DiMauro	36
20	Overproduction of dihydrofolate reductase by antifolate resistant Chinese hamster cells 1978 ·The Journal of Cell Biology ·Sara Shanske,Peter W. Melera,June L. Biedler	1

About Sara Shanske

Sara Shanske is a scholar working on Clinical Biochemistry, Rheumatology and Molecular Biology, having authored 188 papers that have together received 12.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (126 papers), Metabolism and Genetic Disorders (109 papers) and ATP Synthase and ATPases Research (61 papers). The work is most often cited by research in Clinical Biochemistry (6.2k citations), Molecular Biology (9.6k citations) and Rheumatology (1.5k citations). Sara Shanske has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include S. DiMauro, Salvatore DiMauro, Eric A. Schon, Carlos T. Moraes, Eduardo Bonilla, Michio Hirano, Filippo M. Santorelli, Seiichi Tsujino, Kurenai Tanji and Carolyn M. Sue. Their work appears in journals such as Nature, New England Journal of Medicine and The Lancet.

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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