Garrett Gotway

1.1k total citations
16 papers, 479 citations indexed

About

Garrett Gotway is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Garrett Gotway has authored 16 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Garrett Gotway's work include Genomics and Rare Diseases (6 papers), Metabolism and Genetic Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Garrett Gotway is often cited by papers focused on Genomics and Rare Diseases (6 papers), Metabolism and Genetic Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Garrett Gotway collaborates with scholars based in United States, Canada and United Arab Emirates. Garrett Gotway's co-authors include L. Aravind, Roger A. Schultz, Valerie L. Gerlach, Eugene V. Koonin, Errol C. Friedberg, Jason Y. Park, Juan M. Pascual, Rüdiger Schultz, Jeffrey A. SoRelle and R.L. Eddy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Clinical Chemistry and The Journal of Pediatrics.

In The Last Decade

Garrett Gotway

16 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Garrett Gotway United States	8	322	144	66	44	40	16	479
Elena Schnabel‐Besson Germany	8	348 1.1×	110 0.8×	13 0.2×	23 0.5×	62 1.6×	17	582
Kumiko Ohkubo Japan	10	225 0.7×	66 0.5×	32 0.5×	43 1.0×	61 1.5×	22	395
Kristen Wigby United States	10	163 0.5×	190 1.3×	49 0.7×	18 0.4×	24 0.6×	25	376
Amelie S. Lotz‐Havla Germany	12	207 0.6×	33 0.2×	37 0.6×	98 2.2×	17 0.4×	25	396
Kathryn E. Dickerson United States	10	602 1.9×	119 0.8×	79 1.2×	10 0.2×	52 1.3×	23	786
Briana Vecchio-Pagán United States	11	164 0.5×	82 0.6×	37 0.6×	4 0.1×	17 0.4×	15	386
Marcia L. Padilla United States	11	163 0.5×	109 0.8×	18 0.3×	17 0.4×	17 0.4×	13	474
Wai Kit United States	14	570 1.8×	25 0.2×	165 2.5×	11 0.3×	34 0.8×	32	772
Shane C. Quinonez United States	11	221 0.7×	172 1.2×	42 0.6×	60 1.4×	23 0.6×	29	396
Harold H. Harrison United States	12	256 0.8×	51 0.4×	13 0.2×	18 0.4×	20 0.5×	27	408

Countries citing papers authored by Garrett Gotway

Since Specialization

Citations

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

Fields of papers citing papers by Garrett Gotway

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Garrett Gotway

This figure shows the co-authorship network connecting the top 25 collaborators of Garrett Gotway. A scholar is included among the top collaborators of Garrett Gotway 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 Garrett Gotway. Garrett Gotway 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

Pachnis, Panayotis, et al.. (2023). Partial N‐acetyl glutamate synthase deficiency presenting as postpartum hyperammonemia: Diagnosis and subsequent pregnancy management. JIMD Reports. 64(6). 403–409. 2 indexed citations

Harris, Robert C., Panayotis Pachnis, Hongli Chen, et al.. (2023). Novel pathogenicUQCRC2variants in a female with normal neurodevelopment. Molecular Case Studies. 9(4). a006295–a006295. 2 indexed citations

McNutt, Markey, et al.. (2022). Arginase 1 Deficiency in Patients Initially Diagnosed with Hereditary Spastic Paraplegia. Movement Disorders Clinical Practice. 10(1). 109–114. 5 indexed citations

Wood, W.D., et al.. (2021). The roles of homocysteinemia and methylmalonic acidemia in kidney injury in atypical hemolytic uremic syndrome caused by cobalamin C deficiency. Pediatric Nephrology. 37(6). 1415–1418. 5 indexed citations

Farooqi, Midhat S., et al.. (2020). Reinterpretation of Chromosomal Microarrays with Detailed Medical History. The Journal of Pediatrics. 222. 180–185.e1. 3 indexed citations

SoRelle, Jeffrey A., Juan M. Pascual, Garrett Gotway, & Jason Y. Park. (2020). Assessment of Interlaboratory Variation in the Interpretation of Genomic Test Results in Patients With Epilepsy. JAMA Network Open. 3(4). e203812–e203812. 6 indexed citations

Gotway, Garrett, et al.. (2019). A Novel Homozygous Deletion within the <b><i>FRY</i></b> Gene Associated with Nonsyndromic Developmental Delay. Cytogenetic and Genome Research. 159(1). 19–25. 3 indexed citations

Gotway, Garrett, Julia Kozlitina, Chao Xing, et al.. (2019). Clinical Exome Studies Have Inconsistent Coverage. Clinical Chemistry. 66(1). 199–206. 8 indexed citations

SoRelle, Jeffrey A., et al.. (2018). Clinical Utility of Reinterpreting Previously Reported Genomic Epilepsy Test Results for Pediatric Patients. JAMA Pediatrics. 173(1). e182302–e182302. 45 indexed citations

10.

Dai, Hongzheng, Ayman W. El‐Hattab, Marwan Shinawi, et al.. (2016). FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome. Clinical Genetics. 91(4). 634–639. 19 indexed citations

11.

Stender, Stefan, et al.. (2015). Adult-onset liver disease and hepatocellular carcinoma in S-adenosylhomocysteine hydrolase deficiency. Molecular Genetics and Metabolism. 116(4). 269–274. 33 indexed citations

12.

Agim, Nnenna G., et al.. (2015). IKBKGMutation With Incontinentia Pigmenti and Ring-Enhancing Encephalopathy. JAMA Neurology. 72(12). 1533–1533. 2 indexed citations

13.

Gao, Xiaochong, Garrett Gotway, Karl E. Rathjen, et al.. (2014). Genomic Analyses of Patients With Unexplained Early-Onset Scoliosis. Spine Deformity. 2(5). 324–332. 8 indexed citations

14.

Wang, Jason, Garrett Gotway, Juan M. Pascual, & Jason Y. Park. (2014). Diagnostic Yield of Clinical Next-Generation Sequencing Panels for Epilepsy. JAMA Neurology. 71(5). 650–650. 45 indexed citations

15.

Gerlach, Valerie L., L. Aravind, Garrett Gotway, et al.. (1999). Human and mouse homologs of Escherichia coli DinB (DNA polymerase IV), members of the UmuC/DinB superfamily. Proceedings of the National Academy of Sciences. 96(21). 11922–11927. 165 indexed citations

16.

Eddy, R.L., Vijay S. Tonk, N. Nowak, et al.. (1997). Chromosomal Localization of a Human Mucin Gene (MUC8) and Cloning of the cDNA Corresponding to the Carboxy Terminus. American Journal of Respiratory Cell and Molecular Biology. 16(3). 232–241. 128 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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