Laura Kasch

2.7k total citations
13 papers, 946 citations indexed

About

Laura Kasch is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Laura Kasch has authored 13 papers receiving a total of 946 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in Laura Kasch's work include Neonatal Respiratory Health Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Associations and Epidemiology (2 papers). Laura Kasch is often cited by papers focused on Neonatal Respiratory Health Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Associations and Epidemiology (2 papers). Laura Kasch collaborates with scholars based in United States, Australia and Switzerland. Laura Kasch's co-authors include Stylianos E. Antonarakis, Garry R. Cutting, Beryl J. Rosenstein, H H Kazazian, Julian Zielenski, Lap-Chee Tsui, Haig H. Kazazian, Lap-Chee Tsui, Paula Wolyniec and Ann E. Pulver and has published in prestigious journals such as Nature, New England Journal of Medicine and CHEST Journal.

In The Last Decade

Laura Kasch

13 papers receiving 908 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura Kasch United States	12	400	341	286	102	70	13	946
Gita Akots United States	12	216 0.5×	363 1.1×	405 1.4×	43 0.4×	29 0.4×	14	839
R. Williamson United Kingdom	12	99 0.2×	270 0.8×	341 1.2×	52 0.5×	23 0.3×	27	703
Nathalie Van der Aa Belgium	19	99 0.2×	388 1.1×	412 1.4×	37 0.4×	37 0.5×	26	809
Christine Carlson United States	8	202 0.5×	472 1.4×	874 3.1×	21 0.2×	99 1.4×	8	1.2k
Elly Verbeek Netherlands	12	314 0.8×	120 0.4×	372 1.3×	38 0.4×	17 0.2×	15	901
Rosemarie Smith United States	11	105 0.3×	336 1.0×	409 1.4×	55 0.5×	18 0.3×	21	744
Lawrence C. Layman United States	26	90 0.2×	778 2.3×	762 2.7×	163 1.6×	50 0.7×	76	2.0k
Irene B. M. Konings Netherlands	14	373 0.9×	79 0.2×	859 3.0×	29 0.3×	35 0.5×	16	1.1k
Gülen Eda Ütine Türkiye	14	71 0.2×	373 1.1×	367 1.3×	40 0.4×	28 0.4×	114	715
Rhodora Gacayan United States	8	195 0.5×	281 0.8×	575 2.0×	27 0.3×	61 0.9×	8	850

Countries citing papers authored by Laura Kasch

Since Specialization

Citations

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

Fields of papers citing papers by Laura Kasch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Kasch

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

All Works

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13 of 13 papers shown

1.

Scott, Alan F., David W. Mohr, Laura Kasch, et al.. (2014). Identification of anHMGB3Frameshift Mutation in a Family With an X-linked Colobomatous Microphthalmia Syndrome Using Whole-Genome and X-Exome Sequencing. JAMA Ophthalmology. 132(10). 1215–1215. 18 indexed citations

2.

Hamvas, Aaron, Lawrence M. Nogee, Daniel Wegner, et al.. (2009). Inherited Surfactant Deficiency Caused by Uniparental Disomy of Rare Mutations in the Surfactant Protein-B and ATP Binding Cassette, Subfamily A, Member 3 Genes. The Journal of Pediatrics. 155(6). 854–859.e1. 40 indexed citations

3.

Resar, Jon R., Ariel Roguin, Khurram Nasir, et al.. (2005). Hypoxia-Inducible Factor 1α Polymorphism and Coronary Collaterals in Patients With Ischemic Heart Disease. CHEST Journal. 128(2). 787–791. 95 indexed citations

4.

Zeiger, Joanna S., Terri H. Beaty, Jacqueline B. Hetmanski, et al.. (2002). Genetic and Environmental Risk Factors for Sagittal Craniosynostosis. Journal of Craniofacial Surgery. 13(5). 602–606. 47 indexed citations

5.

Adams, Pamela S., et al.. (2002). Strategies for genotyping: Effectiveness of tailing primers to increase accuracy in short tandem repeat determinations.. PubMed. 13(1). 20–9. 33 indexed citations

6.

Stetten, Gail, Laura Kasch, Alan F. Scott, et al.. (1997). A paternally derived inverted duplication of 7q with evidence of a telomeric deletion. American Journal of Medical Genetics. 68(1). 76–81. 21 indexed citations

7.

Stetten, Gail, Laura Kasch, Alan F. Scott, et al.. (1997). A paternally derived inverted duplication of 7q with evidence of a telomeric deletion. American Journal of Medical Genetics. 68(1). 76–81. 3 indexed citations

8.

Pulver, Ann E., Virginia K. Lasseter, Laura Kasch, et al.. (1995). Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes. American Journal of Medical Genetics. 60(3). 252–260. 202 indexed citations

9.

Karayiorgou, Maria, Laura Kasch, Virginia K. Lasseter, et al.. (1994). Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model. American Journal of Medical Genetics. 54(4). 345–353. 18 indexed citations

10.

Rossiter, Judith Pratt, Karin J. Blakemore, Thomas S. Kickler, et al.. (1994). The use of polymerase chain reaction to determine fetal RhD status. American Journal of Obstetrics and Gynecology. 171(4). 1047–1051. 17 indexed citations

11.

Cutting, Garry R., Laura Kasch, Beryl J. Rosenstein, et al.. (1990). A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. Nature. 346(6282). 366–369. 331 indexed citations

12.

Cutting, Garry R., Laura Kasch, Beryl J. Rosenstein, et al.. (1990). Two Patients with Cystic Fibrosis, Nonsense Mutations in Each Cystic Fibrosis Gene, and Mild Pulmonary Disease. New England Journal of Medicine. 323(24). 1685–1689. 105 indexed citations

13.

Cutting, Garry R., Matthew J. McGinniss, Laura Kasch, Petros Tsipouras, & Stylianos E. Antonarakis. (1990). Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2. Genomics. 8(2). 407–410. 16 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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