L Bachner

957 total citations
14 papers, 712 citations indexed

About

L Bachner is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, L Bachner has authored 14 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in L Bachner's work include Muscle Physiology and Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). L Bachner is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). L Bachner collaborates with scholars based in France, United States and Belgium. L Bachner's co-authors include Peter Donnelly, Jean‐Jacques Schott, P. F. Foley, Éric Drouin, Flavien Charpentier, Gilles Vergnaud, J B Bouhour, A Kahn, K Schärer and Joachim Misselwitz and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and FEBS Letters.

In The Last Decade

L Bachner

14 papers receiving 697 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L Bachner France	10	584	303	223	115	61	14	712
Meriel McEntagart United Kingdom	14	273 0.5×	101 0.3×	149 0.7×	157 1.4×	41 0.7×	24	576
Susan Ludwigsen United States	8	439 0.8×	442 1.5×	98 0.4×	42 0.4×	36 0.6×	9	771
Hannelore Thiele Germany	9	412 0.7×	41 0.1×	256 1.1×	171 1.5×	29 0.5×	13	612
C. Scotton Italy	14	443 0.8×	89 0.3×	73 0.3×	84 0.7×	60 1.0×	20	541
Elizabeth T. DeChene United States	10	405 0.7×	283 0.9×	170 0.8×	53 0.5×	76 1.2×	14	575
Roula Ghaoui Australia	10	300 0.5×	96 0.3×	115 0.5×	131 1.1×	39 0.6×	22	486
M G Sweeney United Kingdom	18	1.0k 1.8×	48 0.2×	85 0.4×	314 2.7×	41 0.7×	21	1.2k
Monica Traverso Italy	13	348 0.6×	61 0.2×	122 0.5×	66 0.6×	81 1.3×	32	488
Veronika Karcagi Hungary	13	461 0.8×	62 0.2×	101 0.5×	79 0.7×	79 1.3×	32	616
Nasim Vasli France	10	353 0.6×	203 0.7×	125 0.6×	78 0.7×	87 1.4×	16	466

Countries citing papers authored by L Bachner

Since Specialization

Citations

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

Fields of papers citing papers by L Bachner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Bachner

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

All Works

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14 of 14 papers shown

Portes, V. des, J.-M. Pinard, Didier Smadja, et al.. (1997). Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.. Journal of Medical Genetics. 34(3). 177–183. 45 indexed citations

Portes, V. des, Pierre Billuart, Alain Carrié, et al.. (1997). A gene for dominant nonspecific X-linked mental retardation is located in Xq28.. PubMed. 60(4). 903–9. 13 indexed citations

Portes, V. des, L Bachner, Thomas Brüls, et al.. (1996). X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter. American Journal of Medical Genetics. 64(1). 69–72. 7 indexed citations

Schott, Jean‐Jacques, Flavien Charpentier, P. F. Foley, et al.. (1995). Mapping of a gene for long QT syndrome to chromosome 4q25-27.. PubMed. 57(5). 1114–22. 276 indexed citations

Kerch, F. El, Abdelaziz Sefiani, K. Azibi, et al.. (1994). Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa.. Journal of Medical Genetics. 31(4). 342–343. 22 indexed citations

Zerres, Klaus, Gabi Mücher, L Bachner, et al.. (1994). Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen. Nature Genetics. 7(3). 429–432. 160 indexed citations

Romero, Norma B., F.M.S. Tomé, France Leturcq, et al.. (1994). Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.. PubMed. 317(1). 70–6. 34 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

Dodé, Catherine, Alexandra Dürr, Christophe Pécheux, et al.. (1993). Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.. PubMed. 316(11). 1374–80. 9 indexed citations

10.

Schweighoffer, Fabien, Pascal Maire, David Tuil, et al.. (1986). In vivo developmental modifications of the expression of genes encoding muscle-specific enzymes in rat.. Journal of Biological Chemistry. 261(22). 10271–10276. 35 indexed citations

11.

Schweighoffer, Fabien, et al.. (1986). Expression of two aldolase A mRNA species in different human and rat tissues. Biochemical Society Transactions. 14(4). 718–719. 1 indexed citations

12.

Raymondjean, Michel, et al.. (1980). Independent expression of cyclic AMP dependent protein kinases related to cyclic nucleotide systems, during triiodothyronine induced cardiac hypertrophy. Life Sciences. 27(5). 387–394. 7 indexed citations

13.

Kneip, Bernard, et al.. (1979). An improved and easy technique for polyamine determination in biological samples. Journal of Chromatography B Biomedical Sciences and Applications. 162(4). 547–559. 11 indexed citations

14.

Thang, M.N., L Bachner, Erik De Clercq, & B. David Stollar. (1977). A continuous high molecular weight base‐paired structure is not an absolute requirement for a potential polynucleotide inducer of interferon. FEBS Letters. 76(2). 159–165. 13 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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