Karen W. Gripp

14.9k total citations · 1 hit paper
140 papers, 5.0k citations indexed

About

Karen W. Gripp is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Karen W. Gripp has authored 140 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 51 papers in Genetics and 24 papers in Immunology. Recurrent topics in Karen W. Gripp's work include Protein Tyrosine Phosphatases (58 papers), Galectins and Cancer Biology (21 papers) and Craniofacial Disorders and Treatments (15 papers). Karen W. Gripp is often cited by papers focused on Protein Tyrosine Phosphatases (58 papers), Galectins and Cancer Biology (21 papers) and Craniofacial Disorders and Treatments (15 papers). Karen W. Gripp collaborates with scholars based in United States, Canada and Germany. Karen W. Gripp's co-authors include Elaine H. Zackai, Katia Sol‐Church, Angela E. Lin, Deborah L. Stabley, Linda K. Nicholson, Elizabeth Hopkins, William B. Dobyns, Catherine A. Stolle, Martin Zenker and Donna M. McDonald‐McGinn and has published in prestigious journals such as Nature Medicine, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Karen W. Gripp

136 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Identifying facial phenotypes of genetic disorders using deep learning

2018 411 citations Martin Zenker, Lynne M. Bird et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karen W. Gripp United States	40	3.4k	1.8k	904	442	426	140	5.0k
Giuseppe Zampino Italy	30	3.1k 0.9×	1.1k 0.6×	1.4k 1.6×	657 1.5×	304 0.7×	184	4.7k
Hirofumi Ohashi Japan	36	3.1k 0.9×	2.5k 1.4×	546 0.6×	385 0.9×	378 0.9×	165	4.8k
Michael A. Patton United Kingdom	36	4.1k 1.2×	1.3k 0.7×	1.5k 1.6×	597 1.4×	236 0.6×	82	6.0k
Martin Zenker Germany	40	4.0k 1.2×	1.9k 1.0×	1.3k 1.5×	1.1k 2.4×	223 0.5×	227	6.3k
Lies H. Hoefsloot Netherlands	45	3.7k 1.1×	1.7k 1.0×	532 0.6×	511 1.2×	324 0.8×	136	6.6k
Kenji Kurosawa Japan	31	1.9k 0.6×	1.5k 0.9×	373 0.4×	211 0.5×	202 0.5×	266	3.7k
Marwan Shinawi United States	32	2.4k 0.7×	1.5k 0.8×	415 0.5×	112 0.3×	396 0.9×	137	4.3k
Hans Scheffer Netherlands	47	3.7k 1.1×	2.7k 1.5×	377 0.4×	341 0.8×	411 1.0×	191	7.9k
Andrew H. Crosby United Kingdom	36	3.9k 1.1×	862 0.5×	1.3k 1.4×	582 1.3×	463 1.1×	125	7.1k
Hirotomo Saitsu Japan	43	4.2k 1.2×	2.8k 1.6×	323 0.4×	473 1.1×	281 0.7×	430	7.7k

Countries citing papers authored by Karen W. Gripp

Since Specialization

Citations

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

Fields of papers citing papers by Karen W. Gripp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karen W. Gripp. 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 Karen W. Gripp. The network helps show where Karen W. Gripp may publish in the future.

Co-authorship network of co-authors of Karen W. Gripp

This figure shows the co-authorship network connecting the top 25 collaborators of Karen W. Gripp. A scholar is included among the top collaborators of Karen W. Gripp 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 Karen W. Gripp. Karen W. Gripp 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

Patel, Nihir, Rafael Dariolli, Simon Ng, et al.. (2024). HRAS -Mutant Cardiomyocyte Model of Multifocal Atrial Tachycardia. Circulation Arrhythmia and Electrophysiology. 17(4). e012022–e012022. 2 indexed citations

Korade, Željka, Allison Anderson, Keri A. Tallman, et al.. (2024). Inhibition of post-lanosterol biosynthesis by fentanyl: potential implications for Fetal Fentanyl Syndrome (FFS). Molecular Psychiatry. 29(12). 3942–3949. 3 indexed citations

Cao, Ye, Eva Fung, Soledad Kleppe, et al.. (2022). Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy. American Journal of Medical Genetics Part A. 191(3). 776–785. 2 indexed citations

Weaver, K. Nicole & Karen W. Gripp. (2022). Central nervous system involvement in individuals withRASopathies. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 190(4). 494–500. 4 indexed citations

Weaver, K. Nicole, Marguerite M. Caré, Yuri A. Zárate, et al.. (2021). Craniosynostosis is a feature of Costello syndrome. American Journal of Medical Genetics Part A. 188(4). 1280–1286. 3 indexed citations

Doja, Asif, Tamara Pringsheim, Brendan F. Andrade, et al.. (2021). Implementation and evaluation of a curriculum on the assessment and treatment of disruptive behaviour disorders. Paediatrics & Child Health. 26(8). 458–461.

Gripp, Karen W., Marni E. Axelrad, Kathryn C. Chatfield, et al.. (2019). Costello syndrome: Clinical phenotype, genotype, and management guidelines. American Journal of Medical Genetics Part A. 179(9). 1725–1744. 72 indexed citations

Gelb, Bruce D., Hélène Cavé, Mitchell W. Dillon, et al.. (2018). ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation. Genetics in Medicine. 20(11). 1334–1345. 90 indexed citations

Schwartz, David D., Jennifer M. Katzenstein, Deborah L. Stabley, et al.. (2017). Age‐related differences in prevalence of autism spectrum disorder symptoms in children and adolescents with Costello syndrome. American Journal of Medical Genetics Part A. 173(5). 1294–1300. 12 indexed citations

10.

Ejaz, Resham, Melissa Carter, & Karen W. Gripp. (2016). Lateral Meningocele Syndrome.

11.

Gripp, Karen W., Laura Baker, Aida Telegrafi, & Kristin G. Monaghan. (2016). The role of objective facial analysis using FDNA in making diagnoses following whole exome analysis. Report of two patients with mutations in the BAF complex genes. American Journal of Medical Genetics Part A. 170(7). 1754–1762. 34 indexed citations

12.

Gripp, Karen W., Laura Baker, Vinay Kandula, et al.. (2016). Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation. American Journal of Medical Genetics Part A. 170(10). 2559–2569. 48 indexed citations

13.

Johnson, Barbara, et al.. (2014). Function and disability in children with Costello syndrome and Cardiofaciocutaneous syndrome. American Journal of Medical Genetics Part A. 167(1). 40–44. 18 indexed citations

14.

Gripp, Karen W., Katherine Robbins, Nara Sobreira, et al.. (2014). Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome. American Journal of Medical Genetics Part A. 167(2). 271–281. 59 indexed citations

15.

Bainbridge, Matthew N., Hao Hu, Donna M. Muzny, et al.. (2013). De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine. 5(2). 11–11. 102 indexed citations

16.

Robbins, Katherine, Deborah L. Stabley, Jennifer Holbrook, Karen W. Gripp, & Katia Sol‐Church. (2013). Uniparental Disomy is Associated with Embryonal Rhabdomyosarcoma in Costello Syndrome and Nonsyndromic Patients: From Core-Side to Bed-Side and Back Again, Impact of Core Laboratories on Biomedical Research. Journal of Biomolecular Techniques JBT. 24. 1 indexed citations

17.

Gripp, Karen W. & Laurie Demmer. (2013). Keratoconus in Costello Syndrome. American Journal of Medical Genetics Part A. 161(5). 1132–1136. 6 indexed citations

18.

Gripp, Karen W., Charles I. Scott, Linda K. Nicholson, et al.. (2008). Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts. American Journal of Medical Genetics Part A. 146A(4). 468–473. 7 indexed citations

19.

Axelrad, Marni E., et al.. (2004). Adaptive skills, cognitive, and behavioral characteristics of Costello syndrome. American Journal of Medical Genetics Part A. 128A(4). 396–400. 34 indexed citations

20.

McDonald‐McGinn, Donna M., Ralph J. DeBerardinis, Sean Bartlett, et al.. (2003). Molecular characterization of Pfeiffer syndrome: Implications for prognosis and genetic counseling.. The American Journal of Human Genetics. 73. 212–212. 1 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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