Kara Weisiger

862 total citations
16 papers, 609 citations indexed

About

Kara Weisiger is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kara Weisiger has authored 16 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kara Weisiger's work include Metabolism and Genetic Disorders (6 papers), Folate and B Vitamins Research (4 papers) and Porphyrin Metabolism and Disorders (2 papers). Kara Weisiger is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Folate and B Vitamins Research (4 papers) and Porphyrin Metabolism and Disorders (2 papers). Kara Weisiger collaborates with scholars based in United States, Canada and Spain. Kara Weisiger's co-authors include George D. Swanson, Richard L. Hughson, Seymour Packman, A. James Barkovich, Gregory M. Enns, Mendel Tuchman, Brenda Eskenazi, Sharon A. Kidd, Andrew J. Wyrobek and Dan H. Moore and has published in prestigious journals such as Neurology, Journal of Applied Physiology and The Journal of Pediatrics.

In The Last Decade

Kara Weisiger

16 papers receiving 580 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kara Weisiger United States	13	235	218	158	118	105	16	609
Hanneke Boon Netherlands	15	409 1.7×	14 0.1×	19 0.1×	53 0.4×	33 0.3×	17	788
Marija Meznarič Slovenia	11	442 1.9×	180 0.8×	23 0.1×	7 0.1×	53 0.5×	26	567
Reynaldo P. Lazaro United States	13	195 0.8×	35 0.2×	17 0.1×	13 0.1×	26 0.2×	23	461
Florence H. J. van Tienen Netherlands	8	271 1.2×	54 0.2×	37 0.2×	14 0.1×	34 0.3×	12	417
Kai Zou United States	18	410 1.7×	10 0.0×	27 0.2×	40 0.3×	29 0.3×	46	716
L Leclerc France	13	192 0.8×	13 0.1×	37 0.2×	9 0.1×	43 0.4×	37	457
Entela Bua United States	8	788 3.4×	192 0.9×	14 0.1×	12 0.1×	21 0.2×	8	1.0k
Yoshiteru Hanai Japan	13	238 1.0×	13 0.1×	11 0.1×	10 0.1×	42 0.4×	25	407
Na Luo China	11	209 0.9×	11 0.1×	15 0.1×	8 0.1×	77 0.7×	25	672

Countries citing papers authored by Kara Weisiger

Since Specialization

Citations

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

Fields of papers citing papers by Kara Weisiger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kara Weisiger

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

All Works

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16 of 16 papers shown

Youngblom, Janey, et al.. (2019). Family Perspectives on Newborn Screening for X-Linked Adrenoleukodystrophy in California. International Journal of Neonatal Screening. 5(4). 42–42. 22 indexed citations

Mendelsohn, Bryce A., Jacque L. Duncan, Anthony T. Moore, et al.. (2018). Cobalamin D Deficiency Identified Through Newborn Screening. JIMD Reports. 44. 73–77. 6 indexed citations

Fernández‐Guerra, Paula, Rosa Navarrete, Kara Weisiger, et al.. (2010). Functional characterization of the novel intronic nucleotide change c.288+9C>T within the BCKDHA gene: understanding a variant presentation of maple syrup urine disease. Journal of Inherited Metabolic Disease. 33(S3). 191–198. 5 indexed citations

Shankar, Suma P., et al.. (2009). 128. Fabry disease: Correlation of progression of white matter disease and severity of neurological manifestations with the pulvinar sign. Molecular Genetics and Metabolism. 96(2). S40–S40. 1 indexed citations

Klein, Ophir D., Dana Kostiner, Kara Weisiger, et al.. (2008). Acute fatal presentation of ornithine transcarbamylase deficiency in a previously healthy male. Hepatology International. 2(3). 390–394. 26 indexed citations

Packman, Wendy, et al.. (2007). Executive functioning in children and adolescents with phenylketonuria. Clinical Genetics. 72(1). 13–18. 52 indexed citations

Slavotinek, Anne, Jill Goldman, Kara Weisiger, et al.. (2005). Marinesco–Sjögren syndrome in a male with mild dysmorphism. American Journal of Medical Genetics Part A. 133A(2). 197–201. 14 indexed citations

Schelley, Susan, et al.. (2005). Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle. Clinical Genetics. 68(4). 337–348. 26 indexed citations

Takanashi, Jun‐ichi, A. James Barkovich, Kara Weisiger, et al.. (2003). Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders.. American Journal of Neuroradiology. 24(6). 1184–7. 71 indexed citations

10.

Sheen, Volney, James W. Wheless, Adria Bodell, et al.. (2003). Periventricular heterotopia associated with chromosome 5p anomalies. Neurology. 60(6). 1033–1036. 76 indexed citations

11.

Eskenazi, Brenda, Andrew J. Wyrobek, Sharon A. Kidd, et al.. (2002). Sperm aneuploidy in fathers of children with paternally and maternally inherited Klinefelter syndrome. Human Reproduction. 17(3). 576–583. 63 indexed citations

12.

Enns, Greg, Raili Seppälä, Kara Weisiger, et al.. (2001). Clinical course and biochemistry of sialuria. Journal of Inherited Metabolic Disease. 24(3). 328–336. 20 indexed citations

13.

Enns, Gregory M., Malcolm J. Bennett, Charles L. Hoppel, et al.. (2000). Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. The Journal of Pediatrics. 136(2). 251–254. 37 indexed citations

14.

Enns, Gregory M., et al.. (1999). Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalamin. Journal of Inherited Metabolic Disease. 22(5). 599–607. 43 indexed citations

15.

Inman, Mark D., Richard L. Hughson, Kara Weisiger, & George D. Swanson. (1987). Estimate of mean tissue O2 consumption at onset of exercise in males. Journal of Applied Physiology. 63(4). 1578–1585. 25 indexed citations

16.

Hughson, Richard L., Kara Weisiger, & George D. Swanson. (1987). Blood lactate concentration increases as a continuous function in progressive exercise. Journal of Applied Physiology. 62(5). 1975–1981. 122 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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