G Morin
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Sensory Systems top 10%
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 3
- Congenital Ear and Nasal Anomalies 3
- Genetics and Neurodevelopmental Disorders 3
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- Hedgehog Signaling Pathway Studies 3
- Ion channel regulation and function 2
- RNA modifications and cancer 2
- Co-authors
- Lise Rodat‐Despoix (1 shared paper)Ahmed Ahidouch (1 shared paper)Fabrice Matifat (1 shared paper)Halima Ouadid‐Ahidouch (1 shared paper)Petra I. Knaus (1 shared paper)Jan H. Boergermann (1 shared paper)Stefan Mundlos (1 shared paper)Petra Seemann (1 shared paper)
- Journals
- Human Mutation (4 papers)European Journal of Medical Genetics (3 papers)European Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)Clinical Journal of the American Society of Nephrology (1 paper)
- Partner nations
- FranceUnited KingdomBelgium
In The Last Decade
G Morin
36 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 76
- Genetics 393
- Sensory Systems 53
- Developmental Biology 23
- Molecular Biology 643
- Genetics 85
Countries citing papers authored by G Morin
This map shows the geographic impact of G Morin'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 G Morin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G Morin more than expected).
Fields of papers citing papers by G Morin
This network shows the impact of papers produced by G Morin. 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 G Morin. The network helps show where G Morin may publish in the future.
Co-authors
The 25 scholars most cited alongside G Morin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 192 | |
| 2 | 2014 | 119 | |
| 3 | 2006 | 115 | |
| 4 | 2019 | 90 | |
| 5 | 2015 | 88 | |
| 6 | 2008 | 58 | |
| 7 | 2011 | 54 | |
| 8 | 2006 | 52 | |
| 9 | 2015 | 49 | |
| 10 | 2014 | 49 | |
| 11 | 2012 | 41 | |
| 12 | 2017 | 41 | |
| 13 | 2019 | 35 | |
| 14 | 2017 | 30 | |
| 15 | Hereditary gallbladder agenesis: twelve cases in the same family. | 1972 | 28 |
| 16 | 2015 | 18 | |
| 17 | 1993 | 15 | |
| 18 | 2003 | 14 | |
| 19 | 2015 | 12 | |
| 20 | 2001 | 9 |
About G Morin
G Morin is a scholar working on Genetics, Genetics, Molecular Biology, Dermatology and Developmental Biology, having authored 41 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Inflammatory Myopathies and Dermatomyositis (4 papers), Genomics and Rare Diseases (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Ion channel regulation and function (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Genetics (393 citations), Sensory Systems (53 citations), Developmental Biology (23 citations), Molecular Biology (643 citations) and Genetics (85 citations). G Morin has collaborated with scholars based in France, United Kingdom and Belgium. Frequent co-authors include Lise Rodat‐Despoix, Ahmed Ahidouch, Fabrice Matifat, Halima Ouadid‐Ahidouch, Petra I. Knaus, Jan H. Boergermann, Stefan Mundlos, Petra Seemann, Katarina Lehmann and RONALD W. TAYLOR. Their work appears in journals such as Human Mutation, European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics and Clinical Journal of the American Society of Nephrology.
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.