Laura Konczal

524 total citations
13 papers, 185 citations indexed

About

Laura Konczal is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Laura Konczal has authored 13 papers receiving a total of 185 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Laura Konczal's work include Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (5 papers) and Amino Acid Enzymes and Metabolism (2 papers). Laura Konczal is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (5 papers) and Amino Acid Enzymes and Metabolism (2 papers). Laura Konczal collaborates with scholars based in United States, Canada and France. Laura Konczal's co-authors include Kosuke Izumi, Marilyn C. Jones, Anna L. Mitchell, Beth A. Kaminski, Naveen Uli, Shawn E. McCandless, Maninder Kaur, Carol A. Crowe, Laird G. Jackson and Małgorzata J.M. Nowaczyk and has published in prestigious journals such as The Journal of Pediatrics, Journal of Medical Genetics and Molecular Genetics and Metabolism.

In The Last Decade

Laura Konczal

13 papers receiving 183 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Konczal United States 6 119 77 34 30 19 13 185
Shahida Moosa South Africa 10 91 0.8× 96 1.2× 10 0.3× 8 0.3× 16 0.8× 29 169
Joseph W. Ray United States 8 56 0.5× 52 0.7× 16 0.5× 20 0.7× 35 1.8× 16 116
Yasufumi Ohtsuka Japan 9 68 0.6× 78 1.0× 10 0.3× 3 0.1× 10 0.5× 20 228
Oğuz Çilingir Türkiye 8 47 0.4× 87 1.1× 10 0.3× 8 0.3× 14 0.7× 39 166
Willa Thorson United States 5 50 0.4× 54 0.7× 14 0.4× 6 0.2× 39 2.1× 12 132
Stacey Hume Canada 10 68 0.6× 108 1.4× 23 0.7× 29 1.0× 9 0.5× 19 207
Zita Halász Hungary 8 164 1.4× 131 1.7× 18 0.5× 9 0.3× 20 1.1× 20 267
Lutz Pfeiffer Germany 6 141 1.2× 69 0.9× 15 0.4× 3 0.1× 22 1.2× 6 192
Lucile Boutaud France 8 79 0.7× 133 1.7× 45 1.3× 8 0.3× 9 0.5× 20 233
Joanna Lazier Canada 8 67 0.6× 46 0.6× 10 0.3× 9 0.3× 21 1.1× 19 126

Countries citing papers authored by Laura Konczal

Since Specialization
Citations

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

Fields of papers citing papers by Laura Konczal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Konczal

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

All Works

13 of 13 papers shown
1.
Harding, Cary O., Janet Thomas, María L. Couce, et al.. (2025). P171: Durable efficacy and safety of DTX301: Long-term follow up of a phase 1/2 trial in adults with ornithine transcarbamylase deficiency*. Genetics in Medicine Open. 3. 102136–102136. 2 indexed citations
2.
Thomas, Janet, Wen‐Hann Tan, Aneal Khan, et al.. (2024). Long-term safety and efficacy of DTX301 in adults with late-onset ornithine transcarbamylase (OTC) deficiency: A Phase 1/2 trial. Molecular Genetics and Metabolism. 141(4). 108266–108266. 1 indexed citations
3.
4.
Waisbren, Susan E., Barbara K. Burton, Annette Feigenbaum, et al.. (2021). Long-term preservation of intellectual functioning in sapropterin-treated infants and young children with phenylketonuria: A seven-year analysis. Molecular Genetics and Metabolism. 132(2). 119–127. 11 indexed citations
5.
Konczal, Laura, et al.. (2021). Idiopathic chronic pancreatitis treated with ivacaftor in a CFTR carrier with methylmalonic acidemia. Journal of Cystic Fibrosis. 21(4). 603–605. 2 indexed citations
6.
McCandless, Shawn E., et al.. (2021). A novel cause of emergent hyperammonemia: Cryptococcal fungemia and meningitis. Molecular Genetics and Metabolism Reports. 29. 100825–100825. 5 indexed citations
7.
Rötig, Agnès, Charles‐Joris Roux, R. Lévy, et al.. (2020). Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?. Journal of Medical Genetics. 59(2). 204–208. 5 indexed citations
8.
Zacharias, M., et al.. (2019). Life-threatening presentations of propionic acidemia due to the Amish PCCB founder variant. Molecular Genetics and Metabolism Reports. 21. 100537–100537. 6 indexed citations
9.
Konczal, Laura, et al.. (2016). Challenges in the diagnosis and management of disorders of sex development. Birth Defects Research Part C Embryo Today Reviews. 108(4). 293–308. 15 indexed citations
10.
Tarini, Beth A., Laura Konczal, Aaron J. Goldenberg, Edward B. Goldman, & Shawn E. McCandless. (2013). The Perils of SNP Microarray Testing: Uncovering Unexpected Consanguinity. Pediatric Neurology. 49(1). 50–53. 5 indexed citations
11.
Slavin, Thomas P., Noam Lazebnik, Dinah Clark, et al.. (2012). Germline mosaicism in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 158A(6). 1481–1485. 23 indexed citations
12.
Izumi, Kosuke, Laura Konczal, Anna L. Mitchell, & Marilyn C. Jones. (2011). Underlying Genetic Diagnosis of Pierre Robin Sequence: Retrospective Chart Review at Two Children’s Hospitals and a Systematic Literature Review. The Journal of Pediatrics. 160(4). 645–650.e2. 98 indexed citations
13.
Dyke, Peter C., Laura Konczal, Dennis Bartholomew, Kim L. McBride, & Timothy M. Hoffman. (2008). Acute Dilated Cardiomyopathy in a Patient with Deficiency of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase. Pediatric Cardiology. 30(4). 523–526. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Shahida Moosa Breakdown of academic impact, for papers by Joseph W. Ray Breakdown of academic impact, for papers by Yasufumi Ohtsuka Breakdown of academic impact, for papers by Oğuz Çilingir Breakdown of academic impact, for papers by Willa Thorson Breakdown of academic impact, for papers by Stacey Hume Breakdown of academic impact, for papers by Zita Halász Breakdown of academic impact, for papers by Lutz Pfeiffer Breakdown of academic impact, for papers by Lucile Boutaud Breakdown of academic impact, for papers by Joanna Lazier
Rankless by CCL
2026