H Drac

409 total citations
38 papers, 293 citations indexed

About

H Drac is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Neurology. According to data from OpenAlex, H Drac has authored 38 papers receiving a total of 293 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Cellular and Molecular Neuroscience, 13 papers in Cell Biology and 12 papers in Neurology. Recurrent topics in H Drac's work include Hereditary Neurological Disorders (18 papers), Peripheral Neuropathies and Disorders (8 papers) and Cellular Mechanics and Interactions (6 papers). H Drac is often cited by papers focused on Hereditary Neurological Disorders (18 papers), Peripheral Neuropathies and Disorders (8 papers) and Cellular Mechanics and Interactions (6 papers). H Drac collaborates with scholars based in Poland, United Kingdom and United States. H Drac's co-authors include H Jedrzejowska, I Hausmanowa-Pétrusewicz, Andrzej Kochański, Dagmara Kabzińska, K Rowińska-Marcińska, Barbara Ryniewicz, M. Jenkison, Rachael W. Taylor, Lester S. Adelman and Walter G. Bradley and has published in prestigious journals such as Neurology, Acta Neuropathologica and Journal of the Neurological Sciences.

In The Last Decade

H Drac

35 papers receiving 287 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H Drac Poland 10 183 133 75 68 63 38 293
R. Liane Ramirez United States 8 259 1.4× 247 1.9× 23 0.3× 62 0.9× 116 1.8× 11 366
Marvin P. Rozear United States 12 317 1.7× 116 0.9× 137 1.8× 38 0.6× 259 4.1× 18 540
Gautam Wali Australia 12 169 0.9× 119 0.9× 77 1.0× 50 0.7× 103 1.6× 30 363
Qiubo Jiang Canada 5 105 0.6× 95 0.7× 72 1.0× 32 0.5× 75 1.2× 8 248
Shintaro Otsuka Japan 6 86 0.5× 63 0.5× 26 0.3× 22 0.3× 38 0.6× 9 204
Michiel R. Fokkens Netherlands 9 176 1.0× 206 1.5× 47 0.6× 17 0.3× 64 1.0× 11 312
Hiroshi Nishiye Japan 10 132 0.7× 144 1.1× 11 0.1× 72 1.1× 23 0.4× 20 436
Stacey Nee MacFarlane United States 6 291 1.6× 312 2.3× 81 1.1× 24 0.4× 9 0.1× 7 429
Michel Meijer Netherlands 8 184 1.0× 204 1.5× 154 2.1× 17 0.3× 39 0.6× 8 385
Isabel Banchs Spain 11 309 1.7× 229 1.7× 84 1.1× 18 0.3× 117 1.9× 19 424

Countries citing papers authored by H Drac

Since Specialization
Citations

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

Fields of papers citing papers by H Drac

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Drac

This figure shows the co-authorship network connecting the top 25 collaborators of H Drac. A scholar is included among the top collaborators of H Drac 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 H Drac. H Drac 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.
Lipowska, Marta, H Drac, Dorota Rowczenio, et al.. (2020). Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) in Poland — genetic and clinical presentation. Neurologia i Neurochirurgia Polska. 54(6). 552–560. 3 indexed citations
2.
Potulska‐Chromik, Anna, Elena Sinkiewicz‐Darol, Anna Kostera‐Pruszczyk, et al.. (2012). Original article Charcot-Marie-Tooth type 1C disease coexisting with progressive multiple sclerosis: a study of an overlapping syndrome. Folia Neuropathologica. 4(4). 369–374. 5 indexed citations
3.
Kabzińska, Dagmara, Axel Niemann, H Drac, et al.. (2011). A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C disease. Neurogenetics. 12(2). 145–153. 15 indexed citations
4.
Drac, H, et al.. (2010). Dysmyelinating and demyelinating Charcot–Marie–Tooth disease associated with two myelin protein zero gene mutations. Journal of Applied Genetics. 52(2). 177–183. 5 indexed citations
5.
Drac, H, et al.. (2010). Familial partial lipodystrophy associated with the heterozygous LMNA mutation 1445G>A (Arg482Gln) in a Polish family. Neurologia i Neurochirurgia Polska. 44(3). 291–296. 7 indexed citations
6.
Jędrzejowska, Maria, Barbara Ryniewicz, Dagmara Kabzińska, et al.. (2008). A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3). Neuromuscular Disorders. 18(4). 339–341. 6 indexed citations
7.
Kabzińska, Dagmara, et al.. (2007). Late‐onset Charcot‐Marie‐Tooth type 2 disease with hearing impairment associated with a novel Pro105Thr mutation in the MPZ gene. American Journal of Medical Genetics Part A. 143A(18). 2196–2199. 15 indexed citations
8.
Kabzińska, Dagmara, Raül Pérez‐Ollé, H Drac, et al.. (2006). Is a novel I214M substitution in the NEFL gene a cause of Charcot‐Marie‐Tooth disease? Functional analysis using cell culture models. Journal of the Peripheral Nervous System. 11(3). 225–231. 8 indexed citations
9.
Kabzińska, Dagmara, Andrzej Kochański, H Drac, et al.. (2005). Autosomal Recessive Axonal Form of Charcot-Marie-Tooth Disease Caused by Compound Heterozygous 3′-Splice Site and Ser130Cys Mutation in theGDAP1Gene. Neuropediatrics. 36(3). 206–209. 10 indexed citations
10.
Kabzińska, Dagmara, Andrzej Kochański, H Drac, et al.. (2005). A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot–Marie–Tooth type 4 disease. Journal of the Neurological Sciences. 241(1-2). 7–11. 7 indexed citations
11.
Kochański, Andrzej, H Drac, Dagmara Kabzińska, & I Hausmanowa-Pétrusewicz. (2004). A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin. Neuromuscular Disorders. 14(3). 229–232. 6 indexed citations
12.
Kochański, Andrzej, Dagmara Kabzińska, H Drac, et al.. (2004). Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene. European Journal of Paediatric Neurology. 8(4). 221–224. 3 indexed citations
13.
Kochański, Andrzej, H Drac, H Jedrzejowska, & I Hausmanowa-Pétrusewicz. (2003). Focally folded myelin in Charcot–Marie–Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report. European Journal of Neurology. 10(5). 547–549. 11 indexed citations
14.
Fidziańska, Anna, H Drac, & J Rafałowska. (2002). Phenomenon of Schwann cell apoptosis in a case of congenital hypomyelinating neuropathy with basal lamina onion bulb formation. Brain and Development. 24(7). 727–731. 2 indexed citations
15.
Fidziańska, Anna, H Drac, & Anna Kamińska. (1999). Familial inclusion body myopathy with desmin storage. Acta Neuropathologica. 97(5). 509–514. 15 indexed citations
16.
Rafałowska, J, et al.. (1995). Coexistence of various vascular malformations within the brain.. PubMed. 33(4). 247–50. 2 indexed citations
17.
Rowińska-Marcińska, K, Elżbieta Szmidt-Sałkowska, Ewa Toporowska‐Kowalska, et al.. (1994). [Diagnostic yield of electrophysiological and immunological studies in inflammatory myopathies].. PubMed. 28(1 Suppl 1). 103–13.
18.
Drac, H, et al.. (1992). Chronic progressive axonal polyneuropathy simulating Guillain-Barré syndrome.. PubMed. 30(1). 81–9. 3 indexed citations
19.
Bradley, Walter G., Rachael W. Taylor, Lester S. Adelman, et al.. (1990). Progressive Myopathy in Hyperkalemic Periodic Paralysis. Archives of Neurology. 47(9). 1013–1017. 63 indexed citations
20.
Drac, H. (1977). [Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy].. PubMed. 15(1). 1–16. 2 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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