Paul Kruszka

3.4k total citations
66 papers, 1.1k citations indexed

About

Paul Kruszka is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Paul Kruszka has authored 66 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 33 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Paul Kruszka's work include Hedgehog Signaling Pathway Studies (16 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genomics and Rare Diseases (9 papers). Paul Kruszka is often cited by papers focused on Hedgehog Signaling Pathway Studies (16 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genomics and Rare Diseases (9 papers). Paul Kruszka collaborates with scholars based in United States, Nigeria and Canada. Paul Kruszka's co-authors include Maximilian Muenke, Josef M. Miller, Richard A. Altschuler, Yehoash Raphael, Ariel F. Martinez, Adebowale Adeyemo, Yonit A. Addissie, Cedrik Tekendo‐Ngongang, Debra S. Regier and Karin Weiss and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Paul Kruszka

62 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul Kruszka United States 20 453 397 197 138 121 66 1.1k
Sandra Janssens Belgium 20 483 1.1× 430 1.1× 129 0.7× 293 2.1× 83 0.7× 66 1.5k
Hubert Journel France 23 563 1.2× 559 1.4× 71 0.4× 191 1.4× 55 0.5× 57 1.4k
Christina Chen United States 21 343 0.8× 122 0.3× 91 0.5× 44 0.3× 84 0.7× 48 1.4k
Rena E. Falk United States 19 408 0.9× 447 1.1× 86 0.4× 174 1.3× 84 0.7× 39 1.0k
W E Nance United States 21 613 1.4× 323 0.8× 165 0.8× 163 1.2× 48 0.4× 48 1.4k
Judith P. Willner United States 14 631 1.4× 527 1.3× 55 0.3× 191 1.4× 73 0.6× 33 1.2k
Valentina Mancini Italy 20 192 0.4× 188 0.5× 44 0.2× 41 0.3× 146 1.2× 73 1.1k
Ingele Casteels Belgium 23 542 1.2× 315 0.8× 28 0.1× 310 2.2× 311 2.6× 123 1.8k
Klaus Kjaer Denmark 23 887 2.0× 557 1.4× 52 0.3× 101 0.7× 38 0.3× 59 1.6k
Yolanda Martín Spain 15 310 0.7× 59 0.1× 146 0.7× 39 0.3× 111 0.9× 45 940

Countries citing papers authored by Paul Kruszka

Since Specialization
Citations

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

Fields of papers citing papers by Paul Kruszka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Kruszka

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

All Works

20 of 20 papers shown
1.
Morrow, Michelle, Erin Torti, Kirsty McWalter, et al.. (2024). MGA-related syndrome: A proposed novel disorder. Human Genetics and Genomics Advances. 6(1). 100387–100387.
2.
Timberlake, Andrew T., Garrett Allington, Emre Kiziltug, et al.. (2023). De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis. The American Journal of Human Genetics. 110(5). 846–862. 11 indexed citations
3.
Addissie, Yonit A., Paul Kruszka, Zoë C. Wong, et al.. (2020). Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study. Environmental Health. 19(1). 65–65. 27 indexed citations
4.
Kruszka, Paul & Andrea Beaton. (2020). The state of congenital heart disease. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 5–6. 5 indexed citations
5.
Mzoughi, Slim, Diana Low, Sheena L. M. Ong, et al.. (2020). PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly. Science Advances. 6(2). eaax9852–eaax9852. 9 indexed citations
6.
Jain, Mahim, et al.. (2020). Genetic screening for hypertrophic cardiomyopathy in large, asymptomatic military cohorts. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 124–128. 3 indexed citations
7.
Tekendo‐Ngongang, Cedrik, Paul Kruszka, Ariel F. Martinez, & Maximilian Muenke. (2019). Novel heterozygous variants in KMT2D associated with holoprosencephaly. Clinical Genetics. 96(3). 266–270. 12 indexed citations
8.
Beaton, Andrea, et al.. (2019). The genetic workup for structural congenital heart disease. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 178–186. 17 indexed citations
9.
Hu, Ping, Ariel F. Martinez, Paul Kruszka, et al.. (2018). Low-level parental mosaicism affects the recurrence risk of holoprosencephaly. Genetics in Medicine. 21(4). 1015–1020. 9 indexed citations
10.
Weiss, Karin, Paul Kruszka, Eric Levey, & Maximilian Muenke. (2018). Holoprosencephaly from conception to adulthood. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(2). 122–127. 15 indexed citations
11.
Kruszka, Paul, Ariel F. Martinez, Jeffrey E. Ming, et al.. (2018). Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(2). 175–186. 3 indexed citations
12.
Martinez, Ariel F., Yu Abe, Paul Kruszka, et al.. (2017). Human germline hedgehog pathway mutations predispose to fatty liver. Journal of Hepatology. 67(4). 809–817. 25 indexed citations
13.
Berger, Seth, Karin Weiss, Ariel F. Martinez, et al.. (2017). SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly. Congenital Anomalies. 58(1). 29–32. 10 indexed citations
14.
Kruszka, Paul, Yonit A. Addissie, Donald W. Hadley, et al.. (2016). Muenke syndrome: An international multicenter natural history study. American Journal of Medical Genetics Part A. 170(4). 918–929. 31 indexed citations
15.
Bonham, Vence L., Benjamin E. Berkman, Paul Kruszka, et al.. (2016). Towards a more representative morphology: clinical and ethical considerations for including diverse populations in diagnostic genetic atlases. Genetics in Medicine. 18(11). 1069–1074. 21 indexed citations
16.
Muenke, Maximilian, et al.. (2015). Congenital Heart Disease. 9 indexed citations
17.
Kruszka, Paul, Brian Kirmse, Dina J. Zand, et al.. (2014). Concurrent non-ketotic hyperglycinemia and propionic acidemia in an eight year old boy. Molecular Genetics and Metabolism Reports. 1. 237–240. 5 indexed citations
18.
Kruszka, Paul, Irini Manoli, Jennifer L. Sloan, Jeffrey B. Kopp, & Charles P. Venditti. (2013). Renal growth in isolated methylmalonic acidemia. Genetics in Medicine. 15(12). 990–996. 30 indexed citations
19.
Kruszka, Paul, et al.. (2009). Diagnosis and management of Sjögren syndrome.. PubMed. 79(6). 465–70. 58 indexed citations
20.
Miller, Josef M., et al.. (1997). Neurotrophins can enhance spiral ganglion cell survival after inner hair cell loss. International Journal of Developmental Neuroscience. 15(4-5). 631–643. 240 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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