L Bachner
Impact in
-
- Cardiac electrophysiology and arrhythmias
- Cardiomyopathy and Myosin Studies
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
Papers in
-
- Muscle Physiology and Disorders 4
- Ion channel regulation and function 2
- Mitochondrial Function and Pathology 2
- RNA modifications and cancer 2
- Ubiquitin and proteasome pathways 2
-
- Amino Acid Enzymes and Metabolism 2
- Co-authors
- Gilles Vergnaud (1 shared paper)Flavien Charpentier (1 shared paper)Peter Donnelly (1 shared paper)J B Bouhour (1 shared paper)Éric Drouin (1 shared paper)Jean‐Jacques Schott (1 shared paper)P. F. Foley (1 shared paper)Sabine Rudnik (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Human Molecular Genetics (1 paper)Biochemical Society Transactions (1 paper)FEBS Letters (1 paper)Journal of Biological Chemistry (1 paper)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
L Bachner
14 papers receiving 741 citations
Peers
Comparison fields: 5 of 61
- Cardiology and Cardiovascular Medicine 328
- Genetics 251
- Molecular Biology 573
- Cellular and Molecular Neuroscience 107
- Developmental Neuroscience 16
Countries citing papers authored by L Bachner
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
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-authors
The 25 scholars most cited alongside L Bachner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Mapping of a gene for long QT syndrome to chromosome 4q25-27. | 1995 | 300 |
| 2 | 1994 | 189 | |
| 3 | 1993 | 87 | |
| 4 | 1997 | 49 | |
| 5 | 1986 | 36 | |
| 6 | Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency. | 1994 | 34 |
| 7 | 1994 | 26 | |
| 8 | 1977 | 16 | |
| 9 | A gene for dominant nonspecific X-linked mental retardation is located in Xq28. | 1997 | 14 |
| 10 | 1979 | 11 | |
| 11 | Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis. | 1993 | 9 |
| 12 | 1980 | 8 | |
| 13 | 1996 | 8 | |
| 14 | 1986 | 1 |
About L Bachner
L Bachner is a scholar working on Molecular Biology, Biochemistry, Genetics, Geriatrics and Gerontology and Cardiology and Cardiovascular Medicine, having authored 14 papers that have together received 788 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Amino Acid Enzymes and Metabolism (2 papers), Ion channel regulation and function (2 papers), Mitochondrial Function and Pathology (2 papers), RNA modifications and cancer (2 papers), Ubiquitin and proteasome pathways (2 papers) and Cardiac electrophysiology and arrhythmias (1 paper). The work is most often cited by research in Cardiology and Cardiovascular Medicine (328 citations), Genetics (251 citations), Molecular Biology (573 citations), Cellular and Molecular Neuroscience (107 citations) and Developmental Neuroscience (16 citations). L Bachner has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Gilles Vergnaud, Flavien Charpentier, Peter Donnelly, J B Bouhour, Éric Drouin, Jean‐Jacques Schott, P. F. Foley, Sabine Rudnik, Michael Knapp and Helena A. Kääriäinen. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Biochemical Society Transactions, FEBS Letters and Journal of Biological Chemistry.
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.