Catherine D. Kashork

3.2k total citations
39 papers, 1.9k citations indexed

About

Catherine D. Kashork is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Catherine D. Kashork has authored 39 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 18 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Catherine D. Kashork's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (10 papers). Catherine D. Kashork is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (10 papers). Catherine D. Kashork collaborates with scholars based in United States, Japan and Lebanon. Catherine D. Kashork's co-authors include Lisa G. Shaffer, Blake C. Ballif, Bassem A. Bejjani, Kyle Sundin, Emily A. Rorem, Reza Saleki, Lorraine Potocki, Heidi A. Heilstedt, Aaron Theisen and Carlos A. Bacino and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and Annals of the New York Academy of Sciences.

In The Last Decade

Catherine D. Kashork

39 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine D. Kashork United States	21	1.4k	794	553	450	106	39	1.9k
Shivanand R. Patil United States	24	1.2k 0.8×	1.2k 1.5×	418 0.8×	269 0.6×	150 1.4×	77	2.2k
Lucille Voullaire Australia	27	1.6k 1.1×	1.2k 1.5×	1.0k 1.8×	787 1.7×	40 0.4×	63	2.6k
Roberto Ciccone Italy	23	956 0.7×	681 0.9×	283 0.5×	270 0.6×	82 0.8×	51	1.4k
J P Fryns Belgium	25	1.2k 0.9×	1.1k 1.4×	430 0.8×	190 0.4×	129 1.2×	90	2.2k
Antonie D. Kline United States	23	936 0.6×	1.5k 1.9×	211 0.4×	177 0.4×	100 0.9×	49	2.0k
Jaakko Leisti Finland	27	873 0.6×	1.1k 1.4×	267 0.5×	103 0.2×	183 1.7×	82	2.1k
Peter M. Kroisel Austria	16	658 0.5×	935 1.2×	148 0.3×	172 0.4×	83 0.8×	38	1.5k
Ron Hochstenbach Netherlands	25	1.1k 0.8×	1.2k 1.5×	446 0.8×	318 0.7×	103 1.0×	49	2.1k
Judith P. Willner United States	14	527 0.4×	631 0.8×	191 0.3×	68 0.2×	159 1.5×	33	1.2k
Teresa Mattina Italy	18	839 0.6×	764 1.0×	181 0.3×	172 0.4×	78 0.7×	59	1.4k

Countries citing papers authored by Catherine D. Kashork

Since Specialization

Citations

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

Fields of papers citing papers by Catherine D. Kashork

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine D. Kashork. 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 Catherine D. Kashork. The network helps show where Catherine D. Kashork may publish in the future.

Co-authorship network of co-authors of Catherine D. Kashork

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

All Works

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20 of 20 papers shown

Leggett, J. E., et al.. (2018). A randomized trial of single versus double high-level disinfection of duodenoscopes and linear echoendoscopes using standard automated reprocessing. Gastrointestinal Endoscopy. 88(2). 306–313.e2. 55 indexed citations

Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2011). The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes. Prenatal Diagnosis. 31(8). 778–787. 33 indexed citations

Kashork, Catherine D., Aaron Theisen, & Lisa G. Shaffer. (2010). Diagnosis of Cryptic Chromosomal Syndromes by Fluorescence In Situ Hybridization (FISH). Current Protocols in Human Genetics. 67(1). 2 indexed citations

Kashork, Catherine D., Aaron Theisen, & Lisa G. Shaffer. (2008). Prenatal Diagnosis Using Array CGH. Methods in molecular biology. 444. 59–70. 10 indexed citations

Shaffer, Lisa G., Catherine D. Kashork, Reza Saleki, et al.. (2006). Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases. The Journal of Pediatrics. 149(1). 98–102.e5. 165 indexed citations

Bejjani, Bassem A., Reza Saleki, Blake C. Ballif, et al.. (2005). Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?. American Journal of Medical Genetics Part A. 134A(3). 259–267. 155 indexed citations

Gajęcka, Marzena, Wei Yu, Blake C. Ballif, et al.. (2004). Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure. European Journal of Human Genetics. 13(2). 139–149. 68 indexed citations

Jiang, Yong‐hui, Trilochan Sahoo, Ron C. Michaelis, et al.. (2004). A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A. American Journal of Medical Genetics Part A. 131A(1). 1–10. 112 indexed citations

Mendoza‐Londono, Roberto, et al.. (2004). Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes. Genes Chromosomes and Cancer. 42(1). 82–86. 9 indexed citations

10.

Heilstedt, Heidi A., Blake C. Ballif, Richard A. Lewis, et al.. (2003). Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome. The American Journal of Human Genetics. 72(5). 1200–1212. 181 indexed citations

11.

Heilstedt, Heidi A., Daniel L. Burgess, Aziza Chedrawi, et al.. (2001). Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome. Epilepsia. 42(9). 1103–1111. 65 indexed citations

12.

Inoue, Ken, Makoto Kanai, Yuzo Tanabe, et al.. (2001). Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus–Merzbacher disease. Prenatal Diagnosis. 21(13). 1133–1136. 21 indexed citations

13.

Bacino, Carlos A., Catherine D. Kashork, Nelson Davino, & Lisa G. Shaffer. (2000). Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes. American Journal of Medical Genetics. 92(4). 250–255. 32 indexed citations

14.

Berend, Sue Ann, Aimee S. Spikes, Catherine D. Kashork, et al.. (2000). Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci. American Journal of Medical Genetics. 91(4). 313–313. 2 indexed citations

15.

Tubb, Benjamin, Soraya Bardien, Catherine D. Kashork, et al.. (2000). Characterization of Human Retinal Fascin Gene (FSCN2) at 17q25: Close Physical Linkage of Fascin and Cytoplasmic Actin Genes. Genomics. 65(2). 146–156. 48 indexed citations

16.

Potocki, Lorraine, Sung Sup Park, Marjorie Withers, et al.. (2000). Molecular mechanism for duplication 17p11.2— the homologous recombination reciprocal of the Smith-Magenis microdeletion. Nature Genetics. 24(1). 84–87. 263 indexed citations

17.

Li, Duanxiang, Paula E. Burch, Óscar González‐Lorenzo, et al.. (2000). Molecular Cloning, Expression Analysis, and Chromosome Mapping of WDR6, a Novel Human WD-Repeat Gene. Biochemical and Biophysical Research Communications. 274(1). 117–123. 13 indexed citations

18.

Kashork, Catherine D., Ken‐Shiung Chen, James R. Lupski, & Lisa G. Shaffer. (1999). Prenatal Diagnosis of Charcot‐Marie‐Tooth Disease Type 1A. Annals of the New York Academy of Sciences. 883(1). 457–459. 3 indexed citations

19.

Potocki, Lorraine, Ken‐Shiung Chen, Thearith Koeuth, et al.. (1999). DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome. The American Journal of Human Genetics. 64(2). 471–478. 49 indexed citations

20.

Kashork, Catherine D., James R. Lupski, & Lisa G. Shaffer. (1999). Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescencein situ hybridization. Prenatal Diagnosis. 19(5). 446–449. 15 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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