Jean Welssenbach

476 total citations
8 papers, 387 citations indexed

About

Jean Welssenbach is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Jean Welssenbach has authored 8 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Neurology. Recurrent topics in Jean Welssenbach's work include Genomics and Rare Diseases (2 papers), Neurological diseases and metabolism (2 papers) and RNA regulation and disease (2 papers). Jean Welssenbach is often cited by papers focused on Genomics and Rare Diseases (2 papers), Neurological diseases and metabolism (2 papers) and RNA regulation and disease (2 papers). Jean Welssenbach collaborates with scholars based in France, United States and Italy. Jean Welssenbach's co-authors include J. Beckmann, George W. Padberg, J. De Recondo, Arnold Münnich, Yves Agid, Jamïlé Hazan, Bertrand Fontaine, R.P.M. Bruyn, O. Lyon‐Caen and Alexis Brice and has published in prestigious journals such as Human Molecular Genetics.

In The Last Decade

Jean Welssenbach

8 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean Welssenbach France	8	232	176	92	82	69	8	387
Luba Kalaydjieva Bulgaria	9	267 1.2×	203 1.2×	60 0.7×	113 1.4×	33 0.5×	15	530
Esra Battaloğlu Türkiye	14	231 1.0×	229 1.3×	61 0.7×	126 1.5×	45 0.7×	33	457
Talya Dor Israel	8	176 0.8×	109 0.6×	97 1.1×	60 0.7×	36 0.5×	16	388
Dong-Hui Chen United States	9	370 1.6×	277 1.6×	83 0.9×	39 0.5×	46 0.7×	10	579
Fiorella Speziani United States	9	259 1.1×	252 1.4×	72 0.8×	146 1.8×	71 1.0×	9	529
Kenji Nanao Japan	10	220 0.9×	235 1.3×	80 0.9×	97 1.2×	115 1.7×	17	561
Marie Coutelier France	13	341 1.5×	255 1.4×	107 1.2×	76 0.9×	26 0.4×	15	537
Stéphanie Efthymiou United Kingdom	11	248 1.1×	144 0.8×	136 1.5×	46 0.6×	39 0.6×	60	433
Çiğdem Köroğlu United States	11	151 0.7×	91 0.5×	101 1.1×	58 0.7×	29 0.4×	20	361
Carlos Cervera Spain	13	291 1.3×	86 0.5×	80 0.9×	20 0.2×	143 2.1×	20	465

Countries citing papers authored by Jean Welssenbach

Since Specialization

Citations

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

Fields of papers citing papers by Jean Welssenbach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jean Welssenbach

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

All Works

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8 of 8 papers shown

Fougerousse, Françoise, Odile Broux, Isabelle Richard, et al.. (1994). Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy. Human Molecular Genetics. 3(2). 285–293. 44 indexed citations

Lu-Kuo, Jennifer M., et al.. (1994). Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35. Human Molecular Genetics. 3(1). 99–106. 16 indexed citations

Green, Eric D., Valerie V. Braden, Robert S. Fulton, et al.. (1994). Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. Human Molecular Genetics. 3(3). 489–501. 47 indexed citations

Hazan, Jamïlé, Bertrand Fontaine, R.P.M. Bruyn, et al.. (1994). Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p. Human Molecular Genetics. 3(9). 1569–1573. 105 indexed citations

Frontali, Marina, Francesca Persichetti, Andrea Novelletto, et al.. (1993). The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. Human Molecular Genetics. 2(9). 1383–1387. 19 indexed citations

Kramer, P. L., X.Y. Hauge, J L Weber, et al.. (1993). A microsatellite-based index map of human chromosome 11. Human Molecular Genetics. 2(7). 909–913. 31 indexed citations

Beckmann, J., James Tomfohrde, Robert I. Barnes, et al.. (1993). A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites. Human Molecular Genetics. 2(12). 2019–2030. 46 indexed citations

Bachner, L, J. Beckmann, M. Chaouch, et al.. (1993). Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. Human Molecular Genetics. 2(9). 1423–1428. 79 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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