H. Doose

2.4k total citations
92 papers, 1.7k citations indexed

About

H. Doose is a scholar working on Psychiatry and Mental health, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H. Doose has authored 92 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Psychiatry and Mental health, 18 papers in Clinical Biochemistry and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H. Doose's work include Epilepsy research and treatment (41 papers), Metabolism and Genetic Disorders (18 papers) and Genetics and Neurodevelopmental Disorders (11 papers). H. Doose is often cited by papers focused on Epilepsy research and treatment (41 papers), Metabolism and Genetic Disorders (18 papers) and Genetics and Neurodevelopmental Disorders (11 papers). H. Doose collaborates with scholars based in Germany, Latvia and United Kingdom. H. Doose's co-authors include E Völzke, W. Baier, Bernd A. Neubauer, Stephan Waltz, H.‐J. Christen, H Gerken, D. Scheffner, Göran Carlsson, Ulrich Stephani and Thomas Horstmann and has published in prestigious journals such as The Lancet, Epilepsia and Electroencephalography and Clinical Neurophysiology.

In The Last Decade

H. Doose

85 papers receiving 1.6k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
H. Doose	1.3k	601	599	352	351	92	1.7k
Shunsuke Ohtahara	1.6k 1.2×	668 1.1×	1.0k 1.7×	424 1.2×	344 1.0×	119	2.2k
Eiji Oka	1.5k 1.1×	627 1.0×	883 1.5×	546 1.6×	312 0.9×	111	2.0k
P. Plouin	972 0.7×	444 0.7×	929 1.6×	404 1.1×	238 0.7×	66	1.9k
Michelle Bureau	1.7k 1.3×	763 1.3×	996 1.7×	381 1.1×	448 1.3×	70	2.2k
R. Canger	1.5k 1.1×	464 0.8×	1.1k 1.9×	304 0.9×	319 0.9×	62	2.1k
Dinesh Talwar	978 0.7×	494 0.8×	524 0.9×	298 0.8×	414 1.2×	33	1.7k
Joseph Roger	840 0.6×	414 0.7×	486 0.8×	220 0.6×	198 0.6×	19	1.1k
Jerome Engel	2.0k 1.5×	836 1.4×	885 1.5×	564 1.6×	276 0.8×	25	2.6k
Giuseppe Gobbi	1.2k 0.9×	433 0.7×	649 1.1×	427 1.2×	551 1.6×	85	2.1k
Eija Gaily	1.4k 1.1×	395 0.7×	1.3k 2.1×	356 1.0×	250 0.7×	54	2.3k

Countries citing papers authored by H. Doose

Since Specialization

Citations

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

Fields of papers citing papers by H. Doose

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Doose

This figure shows the co-authorship network connecting the top 25 collaborators of H. Doose. A scholar is included among the top collaborators of H. Doose 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. Doose. H. Doose 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

Joos, Howard A., H. Doose, Ulrich Stephani, et al.. (2005). SCN1A Mutation Analysis in Myoclonic Astatic Epilepsy and Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures. Neuropediatrics. 36(3). 210–213. 37 indexed citations

Doose, H., et al.. (2001). Atypical “Benign” Partial Epilepsy of Childhood or Pseudo-Lennox Syndrome. Part II: Family Study. Neuropediatrics. 32(1). 9–13. 30 indexed citations

Doose, H. & Bernd A. Neubauer. (2001). Preponderance of female sex in the transmission of seizure liability in idiopathic generalized epilepsy. Epilepsy Research. 43(2). 103–114. 14 indexed citations

Stephani, Ulrich & H. Doose. (1999). Benign Idiopathic Partial Epilepsy and Brain Lesion. Epilepsia. 40(3). 373–376. 17 indexed citations

Doose, H., et al.. (1998). Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures. Neuropediatrics. 29(5). 229–238. 45 indexed citations

Doose, H., et al.. (1997). Seizure risk in offspring of individuals with a history of febrile convulsions. European Journal of Pediatrics. 156(6). 476–481. 19 indexed citations

Doose, H., et al.. (1997). Children with Focal Sharp Waves: Clinical and Genetic Aspects. Epilepsia. 38(7). 788–796. 64 indexed citations

Doose, H., Bernd A. Neubauer, & Göran Carlsson. (1996). Children with Benign Focal Sharp Waves in the EEG - Developmental Disorders and Epilepsy. Neuropediatrics. 27(5). 227–241. 65 indexed citations

Whitehouse, William, Ulrike Diebold, Mark I. Rees, et al.. (1993). Exclusion of Linkage of Genetic Focal Sharp Waves to the HLA Region on Chromosome 6p in Families with Benign Partial Epilepsy with Centrotemporal Sharp Waves. Neuropediatrics. 24(4). 208–210. 12 indexed citations

10.

Doose, H., et al.. (1993). Photosensitivity - Genetics and Clinical Significance. Neuropediatrics. 24(5). 249–255. 65 indexed citations

11.

Rees, Mark I., Ulrike Diebold, K L Parker, et al.. (1993). Benign Childhood Epilepsy with Centrotemporal Spikes and the Focal Sharp Wave Trait is not Linked to the Fragile X Region. Neuropediatrics. 24(4). 211–213. 20 indexed citations

12.

Waltz, Stephan, H.‐J. Christen, & H. Doose. (1992). The different patterns of the photoparoxysmal response — a genetic study. Electroencephalography and Clinical Neurophysiology. 83(2). 138–145. 171 indexed citations

13.

Doose, H. & W. Baier. (1989). Benign partial epilepsy and related conditions: Multifactorial pathogenesis with hereditary impairment of brain maturation. European Journal of Pediatrics. 149(3). 152–158. 111 indexed citations

14.

Doose, H.. (1989). Symptomatology in children with focal sharp waves of genetic origin. European Journal of Pediatrics. 149(3). 210–215. 33 indexed citations

15.

Doose, H. & W. Baier. (1987). Epilepsy with primarily generalized myoclonic-astatic seizures: a genetically determined disease. European Journal of Pediatrics. 146(6). 550–554. 20 indexed citations

16.

Gundel, A., W. Baier, & H. Doose. (1981). SPECTRAL ANALYSIS OF EEG IN THE LATE COURSE OF PRIMARY GENERALIZED MYOCLONIC-ASTATIC EPILEPSY¹. Neuropediatrics. 12(2). 110–118. 2 indexed citations

17.

Doose, H., et al.. (1968). Krampfanf�lle nach der Pockenschutzimpfung. European Journal of Pediatrics. 103(3). 214–236. 3 indexed citations

18.

Völzke, E, et al.. (1967). The Treatment of Infantile Spasms and Hypsarrhythmia with Mogadon. Epilepsia. 8(1). 64–70. 33 indexed citations

19.

Doose, H., et al.. (1966). Fieberkrmpfe und Epilepsie: I. tiologie, klinisches Bild und Verlauf der sogenannten Infekt- oder Fieberkrmpfe. 208(4). 400–412. 15 indexed citations

20.

Doose, H., et al.. (1964). [EXPERIENCES WITH OSPOLOT IN THE TREATMENT OF INFANTILE EPILEPSY].. PubMed. 59. 271–4. 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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