Jennifer Skaug

6.0k total citations
11 papers, 1.8k citations indexed

About

Jennifer Skaug is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Jennifer Skaug has authored 11 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Neurology. Recurrent topics in Jennifer Skaug's work include Genetics and Neurodevelopmental Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA and protein synthesis mechanisms (2 papers). Jennifer Skaug is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA and protein synthesis mechanisms (2 papers). Jennifer Skaug collaborates with scholars based in Canada, United States and United Kingdom. Jennifer Skaug's co-authors include Stephen W. Scherer, Péter Szatmári, James S. Sutcliffe, Dalila Pinto, Rainald Moessner, Lonnie Zwaigenbaum, John B. Vincent, Christian R. Marshall, Wendy Roberts and Bridget A. Fernandez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Molecular and Cellular Biology.

In The Last Decade

Jennifer Skaug

11 papers receiving 1.8k citations

Peers

Jennifer Skaug
Susan A. Cook United States
Aldamaria Puliti Italy
Daniela C. Zarnescu United States
Hossein Darvish Iran
Hussein Daoud Canada
Zhengmao Hu China
Marie‐Christine Birling France
Arjan P.M. de Brouwer Netherlands
Gökhan Uyanık Germany
Akiko Iwaki Japan
Susan A. Cook United States
Jennifer Skaug
Citations per year, relative to Jennifer Skaug Jennifer Skaug (= 1×) peers Susan A. Cook

Countries citing papers authored by Jennifer Skaug

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Skaug

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Skaug

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

All Works

11 of 11 papers shown
1.
Moessner, Rainald, Christian R. Marshall, James S. Sutcliffe, et al.. (2007). Contribution of SHANK3 Mutations to Autism Spectrum Disorder. The American Journal of Human Genetics. 81(6). 1289–1297. 494 indexed citations
2.
Lamhonwah, Anne‐Marie, Jennifer Skaug, Stephen W. Scherer, & Ingrid Tein. (2003). A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn’s disease locus (IBD5). Biochemical and Biophysical Research Communications. 301(1). 98–101. 57 indexed citations
3.
Zlotorynski, Eitan, Ayelet Rahat, Jennifer Skaug, et al.. (2003). Molecular Basis for Expression of Common and Rare Fragile Sites. Molecular and Cellular Biology. 23(20). 7143–7151. 199 indexed citations
4.
Wen, Xiao‐Yan, A. Keith Stewart, Jennifer Skaug, Ellen Wei, & Lap-Chee Tsui. (2001). Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to Chromosome 16 but is distinct from the lpd (lipid defect) locus. Mammalian Genome. 12(2). 129–132. 12 indexed citations
5.
6.
Hand, Collette K., Hitoshi Osuga, Yoshiko Yanagisawa, et al.. (2001). A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nature Genetics. 29(2). 166–173. 499 indexed citations
7.
Smith, Annabel N., Jennifer Skaug, Keith A. Choate, et al.. (2000). Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing. Nature Genetics. 26(1). 71–75. 321 indexed citations
8.
Matos, Paulo, Jennifer Skaug, Bárbara Marques, et al.. (2000). Small GTPase Rac1: Structure, Localization, and Expression of the Human Gene. Biochemical and Biophysical Research Communications. 277(3). 741–751. 55 indexed citations
9.
10.
Tonachini, Laura, Roy Morello, Massimiliano Monticone, et al.. (1999). cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP). Cytogenetic and Genome Research. 87(3-4). 191–194. 11 indexed citations
11.
Mansour, Sam J., et al.. (1999). p200 ARF–GEP1: A Golgi-localized guanine nucleotide exchange protein whose Sec7 domain is targeted by the drug brefeldin A. Proceedings of the National Academy of Sciences. 96(14). 7968–7973. 102 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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