G Morin
Impact in
- Developmental Biology top 10%
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 4
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- Hedgehog Signaling Pathway Studies 2
- Epigenetics and DNA Methylation 2
- Ion channel regulation and function 2
- Co-authors
- Halima Ouadid‐Ahidouch (1 shared paper)Fabrice Matifat (1 shared paper)Lise Rodat‐Despoix (1 shared paper)Ahmed Ahidouch (1 shared paper)Petra Knaus (1 shared paper)Petra Seemann (1 shared paper)Jan H. Boergermann (1 shared paper)Stefan Mundlos (1 shared paper)
- Journals
- Human Mutation (2 papers)European Journal of Medical Genetics (2 papers)Journal of Endourology (1 paper)Biochimica et Biophysica Acta (BBA) - Biomembranes (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- FranceUnited KingdomBelgium
In The Last Decade
G Morin
23 papers receiving 336 citations
Peers
Comparison fields: 5 of 54
- Developmental Biology 21
- Sensory Systems 40
- Genetics 153
- Urology 20
- Molecular Biology 204
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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 51 | |
| 2 | 2015 | 48 | |
| 3 | 2006 | 47 | |
| 4 | 2008 | 45 | |
| 5 | 2012 | 41 | |
| 6 | 2017 | 26 | |
| 7 | Hereditary gallbladder agenesis: twelve cases in the same family. | 1972 | 26 |
| 8 | 2015 | 17 | |
| 9 | 2003 | 11 | |
| 10 | 2015 | 11 | |
| 11 | 2001 | 8 | |
| 12 | [Solitary fibrous tumor of the seminal vesicles: apropos of a case]. | 1998 | 6 |
| 13 | The KBG syndrome: an additional sporadic case. | 2000 | 6 |
| 14 | 2022 | 5 | |
| 15 | [Bone and visceral manifestations of lipoatrophic diabetes. Apropos of a case]. | 1992 | 4 |
| 16 | [Intraperitoneal bladder rupture during transurethral resection of the prostate]. | 2003 | 4 |
| 17 | 2018 | 3 | |
| 18 | 2022 | 3 | |
| 19 | 2021 | 2 | |
| 20 | 2024 | 1 |
About G Morin
G Morin is a scholar working on Genetics, Molecular Biology, Surgery, Epidemiology and Rheumatology, having authored 27 papers that have together received 368 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Hedgehog Signaling Pathway Studies (2 papers), Epigenetics and DNA Methylation (2 papers), Urological Disorders and Treatments (2 papers), Inflammatory Myopathies and Dermatomyositis (2 papers), Ion channel regulation and function (2 papers), Urologic and reproductive health conditions (2 papers) and Ureteral procedures and complications (2 papers). The work is most often cited by research in Developmental Biology (21 citations), Sensory Systems (40 citations), Genetics (153 citations), Urology (20 citations) and Molecular Biology (204 citations). G Morin has collaborated with scholars based in France, United Kingdom and Belgium. Frequent co-authors include Halima Ouadid‐Ahidouch, Fabrice Matifat, Lise Rodat‐Despoix, Ahmed Ahidouch, Petra Knaus, Petra Seemann, Jan H. Boergermann, Stefan Mundlos, Katarina Lehmann and Dominique Martin‐Coignard. Their work appears in journals such as Human Mutation, European Journal of Medical Genetics, Journal of Endourology, Biochimica et Biophysica Acta (BBA) - Biomembranes and Molecular Genetics and Metabolism.
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.