Jacek Pilch

1.2k total citations
24 papers, 469 citations indexed

About

Jacek Pilch is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jacek Pilch has authored 24 papers receiving a total of 469 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jacek Pilch's work include Genetic Neurodegenerative Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Neurological diseases and metabolism (3 papers). Jacek Pilch is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Neurological diseases and metabolism (3 papers). Jacek Pilch collaborates with scholars based in Poland, United States and United Kingdom. Jacek Pilch's co-authors include Somayyeh Fahiminiya, Mayana Zatz, Christina Hung, Meire Aguena, Olaf A. Bodamer, Alexandre C. Pereira, Maria Rita Passos‐Bueno, Anna Abramowicz, Guilherme Lopes Yamamoto and Jacek Majewski and has published in prestigious journals such as Neurology, Journal of the Neurological Sciences and Journal of Medical Genetics.

In The Last Decade

Jacek Pilch

22 papers receiving 462 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacek Pilch Poland 12 275 117 117 87 70 24 469
Israel Ben‐Dor Israel 8 304 1.1× 69 0.6× 49 0.4× 41 0.5× 63 0.9× 9 472
R. Cinti Italy 13 280 1.0× 91 0.8× 99 0.8× 30 0.3× 51 0.7× 23 548
Matthias Weider Germany 13 277 1.0× 70 0.6× 61 0.5× 44 0.5× 31 0.4× 21 521
Terra J. Frederick United States 6 171 0.6× 72 0.6× 37 0.3× 51 0.6× 45 0.6× 7 428
Sabrina A. Volpi United States 8 389 1.4× 167 1.4× 48 0.4× 236 2.7× 33 0.5× 9 667
Oleg Lioubinski Germany 7 329 1.2× 182 1.6× 116 1.0× 30 0.3× 24 0.3× 7 580
Ilja Mikenberg Germany 7 209 0.8× 76 0.6× 34 0.3× 71 0.8× 97 1.4× 7 456
Scott E. LeBlanc United States 13 452 1.6× 188 1.6× 56 0.5× 62 0.7× 20 0.3× 13 635
Frédéric Perraud France 10 312 1.1× 158 1.4× 72 0.6× 34 0.4× 29 0.4× 12 519
April Kemper United States 6 188 0.7× 112 1.0× 45 0.4× 119 1.4× 23 0.3× 8 502

Countries citing papers authored by Jacek Pilch

Since Specialization
Citations

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

Fields of papers citing papers by Jacek Pilch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacek Pilch

This figure shows the co-authorship network connecting the top 25 collaborators of Jacek Pilch. A scholar is included among the top collaborators of Jacek Pilch 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 Jacek Pilch. Jacek Pilch 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.
2.
Pilch, Jacek, et al.. (2022). Encephalocraniocutaneous Lipomatosis, a Radiological Challenge: Two Atypical Case Reports and Literature Review. Brain Sciences. 12(12). 1641–1641. 1 indexed citations
3.
Mazurkiewicz‐Bełdzińska, Maria, Anna Kostera‐Pruszczyk, Anna Łusakowska, et al.. (2021). Clinical, multicenter treatment of patients with spinal muscular atrophy - the experience in Poland. 31(60). 11–25.
4.
Szczałuba, Krzysztof, Magdalena Badura‐Stronka, Anna Kutkowska‐Kaźmierczak, et al.. (2021). Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome. Journal of Applied Genetics. 62(3). 477–485. 4 indexed citations
5.
Kotulska, Katarzyna, Ilona Kopyta, Ewa Emich‐Widera, et al.. (2021). Nusinersen treatment of Spinal Muscular Atrophy Type 1 — results of expanded access programme in Poland. Neurologia i Neurochirurgia Polska. 55(3). 289–294. 19 indexed citations
6.
Stępniak, Iwona, Wioletta Krysa, Maria Rakowicz, et al.. (2019). Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes. Neurogenetics. 20(1). 27–38. 33 indexed citations
7.
Sieroń, Aleksander L., et al.. (2018). Mutations in COL1A1 and COL1A2 Genes Associated with Osteogenesis Imperfecta (OI) Types I or III.. Acta Biochimica Polonica. 65(1). 79–86. 20 indexed citations
8.
Pilch, Jacek, Anna Walczak, Victor Murcia Pienkowski, et al.. (2018). Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. Clinical Genetics. 94(3-4). 381–385. 23 indexed citations
9.
Zimowski, Janusz, et al.. (2017). A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene. Journal of Applied Genetics. 58(3). 343–347. 7 indexed citations
10.
Stępniak, Iwona, Wioletta Krysa, Maria Rakowicz, et al.. (2015). Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients. Journal of the Neurological Sciences. 359(1-2). 35–39. 25 indexed citations
11.
Midro, Alina T., Marcella Zollino, Ewa Wiland, et al.. (2015). Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1. Journal of Assisted Reproduction and Genetics. 33(2). 189–197. 2 indexed citations
12.
Iwanowski, Piotr, Barbara Panasiuk, Griet Van Buggenhout, et al.. (2011). Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter. American Journal of Medical Genetics Part A. 155(8). 1833–1847. 4 indexed citations
13.
Zimoń, M., Jonathan Baets, Gian Maria Fabrizi, et al.. (2011). Dominant GDAP1 mutations cause predominantly mild CMT phenotypes. Neurology. 77(6). 540–548. 61 indexed citations
14.
Pilch, Jacek, et al.. (2010). Surveyor Nuclease Detection of Mutations and Polymorphisms of mtDNA in Children. Pediatric Neurology. 43(5). 325–330. 6 indexed citations
15.
Śmigiel, Robert, et al.. (2007). The Pallister-Killian syndrome in a child with rare karyotype—a diagnostic problem. European Journal of Pediatrics. 167(9). 1063–1065. 9 indexed citations
16.
Nawara, Magdalena, Krzysztof Szczałuba, Karine Poirier, et al.. (2006). The ARX mutations: A frequent cause of X‐linked mental retardation. American Journal of Medical Genetics Part A. 140A(7). 727–732. 29 indexed citations
17.
Szczałuba, Krzysztof, Magdalena Nawara, Karine Poirier, et al.. (2006). Genotype-phenotype associations for ARX gene duplication in X-linked mental retardation. Neurology. 67(11). 2073–2075. 14 indexed citations
18.
Iwanowski, Piotr, et al.. (2005). Physical and developmental phenotype analyses in a boy with Wolf-Hirschhorn syndrome.. PubMed. 16(1). 31–40. 3 indexed citations
19.
Pilch, Jacek, et al.. (2002). Topical Review : Friedreich's Ataxia. Journal of Child Neurology. 17(5). 315–319. 13 indexed citations
20.
Pilch, Jacek. (1964). [POLYP OF THE POSTERIOR URETHRA IN A 4-YEAR-OLD BOY].. PubMed. 36. SUPPL:619–21.

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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