Catherine D. Kashork

3.2k citations

39 papers · 1.9k indexed · h-index 21

Genetics top 1%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 2%
Plant Science top 5%
Cognitive Neuroscience top 10%

Co-authors: Lisa G. Shaffer Blake C. Ballif Bassem A. Bejjani Kyle Sundin Emily A. Rorem Reza Saleki Lorraine Potocki Heidi A. Heilstedt
Topics: Genomic variations and chromosomal abnormalities (19 papers)Prenatal Screening and Diagnostics (11 papers)Chromosomal and Genetic Variations (10 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Plant Science
Journals: Nature Genetics Biochemical and Biophysical Research Communications Annals of the New York Academy of Sciences
Partner nations: United States Japan Lebanon

In The Last Decade

Catherine D. Kashork

39 papers receiving 1.8k citations

Peers

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

#	Work	Indexed citations
1	A randomized trial of single versus double high-level disinfection of duodenoscopes and linear echoendoscopes using standard automated reprocessing 2018 ·Gastrointestinal Endoscopy ·(unknown),J. E. Leggett,(unknown),Catherine D. Kashork,Lian Wang,Margret Oethinger,(unknown),(unknown)	55
2	The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes 2011 ·Prenatal Diagnosis ·Lisa G. Shaffer,Justine Coppinger,(unknown),Sarah Alliman,(unknown),Ryan N. Traylor,(unknown),(unknown),Allen N. Lamb,Roger A. Schultz,J. Britt Ravnan,Catherine D. Kashork,Beth S. Torchia,(unknown),Kyle Sundin,(unknown),(unknown),Stephanie Dallaire,Blake C. Ballif	33
3	Prenatal Diagnosis Using Array CGH 2008 ·Methods in molecular biology ·Catherine D. Kashork,Aaron Theisen,Lisa G. Shaffer	10
4	Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases 2006 ·The Journal of Pediatrics ·Lisa G. Shaffer,Catherine D. Kashork,Reza Saleki,Emily A. Rorem,Kyle Sundin,Blake C. Ballif,Bassem A. Bejjani	165
5	Comparative Genomic Hybridization by Microarray for the Detection of Cytogenetic Imbalance 2006 ·Methods in molecular medicine ·Małgorzata Jarmuż‐Szymczak,Blake C. Ballif,Catherine D. Kashork,Aaron Theisen,Bassem A. Bejjani,Lisa G. Shaffer	3
6	Detecting sex chromosome anomalies and common triploidies in products of conception by array‐based comparative genomic hybridization 2006 ·Prenatal Diagnosis ·Blake C. Ballif,Catherine D. Kashork,Reza Saleki,Emily A. Rorem,Kyle Sundin,Bassem A. Bejjani,Lisa G. Shaffer	48
7	Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more? 2005 ·American Journal of Medical Genetics Part A ·Bassem A. Bejjani,Reza Saleki,Blake C. Ballif,Emily A. Rorem,Kyle Sundin,Aaron Theisen,Catherine D. Kashork,Lisa G. Shaffer	155
8	Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure 2004 ·European Journal of Human Genetics ·Marzena Gajęcka,Wei Yu,Blake C. Ballif,Caron D. Glotzbach,(unknown),Chad A. Shaw,Catherine D. Kashork,Heidi A. Heilstedt,(unknown),Aaron Theisen,Ritva Rice,David Rice,Lisa G. Shaffer	68
9	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 2004 ·Genes Chromosomes and Cancer ·Roberto Mendoza‐Londono,Catherine D. Kashork,Lisa G. Shaffer,(unknown),Sharon E. Plon	9
10	A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A 2004 ·American Journal of Medical Genetics Part A ·Yong‐hui Jiang,Trilochan Sahoo,Ron C. Michaelis,Dani Bercovich,Jan Bressler,Catherine D. Kashork,Qian Liu,Lisa G. Shaffer,Richard J. Schroer,David W. Stockton,Richard S. Spielman,Roger E. Stevenson,Arthur L. Beaudet	112
11	Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome 2003 ·The American Journal of Human Genetics ·Heidi A. Heilstedt,Blake C. Ballif,(unknown),Richard A. Lewis,Samuel Stal,Catherine D. Kashork,Carlos A. Bacino,Stuart K. Shapira,Lisa G. Shaffer	181
12	Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation 2002 ·American Journal of Medical Genetics ·André Mégarbané,Bassem A. Bejjani,Lisa G. Shaffer,S Jambart,(unknown),Catherine D. Kashork,Martine Le Merrer	5
13	Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome 2001 ·Epilepsia ·Heidi A. Heilstedt,Daniel L. Burgess,(unknown),Aziza Chedrawi,(unknown),Olivia W. Lee,Catherine D. Kashork,David E. Starkey,Yuanqing Wu,Jeffrey L. Noebels,Lisa G. Shaffer,(unknown)	65
14	Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus–Merzbacher disease 2001 ·Prenatal Diagnosis ·Ken Inoue,Makoto Kanai,Yuzo Tanabe,Takeo Kubota,Catherine D. Kashork,Keiko Wakui,Yoshimitsu Fukushima,James R. Lupski,Lisa G. Shaffer	21
15	Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach 2000 ·European Journal of Human Genetics ·Azra H. Ligon,Catherine D. Kashork,C. Sue Richards,Lisa G. Shaffer	27
16	Molecular Cloning, Expression Analysis, and Chromosome Mapping of WDR6, a Novel Human WD-Repeat Gene 2000 ·Biochemical and Biophysical Research Communications ·Duanxiang Li,Paula E. Burch,Óscar González‐Lorenzo,Catherine D. Kashork,Lisa G. Shaffer,Linda L. Bachinski,Robert Roberts	13
17	Characterization of Human Retinal Fascin Gene (FSCN2) at 17q25: Close Physical Linkage of Fascin and Cytoplasmic Actin Genes 2000 ·Genomics ·Benjamin Tubb,Soraya Bardien,Catherine D. Kashork,Lisa G. Shaffer,Louis S. Ramagli,Jingping Xu,Michael J. Siciliano,Joseph Bryan	48
18	Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescencein situ hybridization 1999 ·Prenatal Diagnosis ·Catherine D. Kashork,James R. Lupski,Lisa G. Shaffer	15
19	DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome 1999 ·The American Journal of Human Genetics ·Lorraine Potocki,Ken‐Shiung Chen,Thearith Koeuth,James M. Killian,Susan T. Iannaccone,Stuart K. Shapira,Catherine D. Kashork,Aimee S. Spikes,Lisa G. Shaffer,James R. Lupski	49
20	Prenatal Diagnosis of Charcot‐Marie‐Tooth Disease Type 1A 1999 ·Annals of the New York Academy of Sciences ·Catherine D. Kashork,Ken‐Shiung Chen,James R. Lupski,Lisa G. Shaffer	3

About Catherine D. Kashork

Catherine D. Kashork is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 39 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (10 papers). The work is most often cited by research in Genetics (1.4k citations), Pediatrics, Perinatology and Child Health (553 citations) and Plant Science (450 citations). Catherine D. Kashork has collaborated with scholars based in United States, Japan and Lebanon. Frequent 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. Their work appears in journals such as Nature Genetics, Biochemical and Biophysical Research Communications and Annals of the New York Academy of Sciences.

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