Corinne Gehrig

4.7k total citations
28 papers, 1.7k citations indexed

About

Corinne Gehrig is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Corinne Gehrig has authored 28 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Genetics and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Corinne Gehrig's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Down syndrome and intellectual disability research (4 papers). Corinne Gehrig is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Down syndrome and intellectual disability research (4 papers). Corinne Gehrig collaborates with scholars based in Switzerland, United States and United Kingdom. Corinne Gehrig's co-authors include Stylianos E. Antonarakis, Robert Lyle, Samuel Deutsch, Jean‐Louis Blouin, Colette Rossier, Maryline Gagnebin, C. Victor Jongeneel, C.D. DeLozier-Blanchet, Michel Guipponi and Maggie Meeks and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Corinne Gehrig

28 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Corinne Gehrig Switzerland	19	983	648	295	225	216	28	1.7k
Marguerite Prieur France	22	789 0.8×	740 1.1×	295 1.0×	245 1.1×	113 0.5×	33	1.5k
Holger Tönnies Germany	23	927 0.9×	833 1.3×	64 0.2×	101 0.4×	141 0.7×	55	1.6k
Evica Rajcan‐Separovic Canada	24	775 0.8×	770 1.2×	111 0.4×	106 0.5×	135 0.6×	58	1.6k
Louise Tee United Kingdom	18	801 0.8×	781 1.2×	153 0.5×	69 0.3×	176 0.8×	31	1.5k
Julie Désir Belgium	19	676 0.7×	529 0.8×	154 0.5×	92 0.4×	85 0.4×	46	1.4k
Karine Hovanes United States	17	978 1.0×	444 0.7×	140 0.5×	93 0.4×	111 0.5×	28	1.9k
Walter Tsark United States	19	1.1k 1.1×	273 0.4×	60 0.2×	195 0.9×	142 0.7×	33	1.4k
Sylvie Taviaux France	21	992 1.0×	312 0.5×	55 0.2×	144 0.6×	213 1.0×	42	1.5k
Alison Condie United Kingdom	22	1.2k 1.2×	472 0.7×	54 0.2×	374 1.7×	743 3.4×	32	1.9k
Antonio Musio Italy	27	2.0k 2.1×	745 1.1×	53 0.2×	182 0.8×	172 0.8×	81	2.5k

Countries citing papers authored by Corinne Gehrig

Since Specialization

Citations

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

Fields of papers citing papers by Corinne Gehrig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Gehrig

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

All Works

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20 of 20 papers shown

1.

Laurent, Sacha, Anne Vannier, Corinne Gehrig, et al.. (2024). Improved variant detection using long-read sequencing and optical mapping: Illustration in STRC-related hearing loss. European Journal of Medical Genetics. 73. 104986–104986. 2 indexed citations

2.

Heurck, Roxane Van, Emmanuelle Ranza, Lina Quteineh, et al.. (2021). Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss. Genes. 12(8). 1277–1277. 13 indexed citations

3.

Guipponi, Michel, Federico Santoni, Maude Schneider, et al.. (2017). No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients. Translational Psychiatry. 7(2). e1039–e1039. 7 indexed citations

4.

Sailani, M. Reza, Federico Santoni, Audrey Letourneau, et al.. (2015). DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins. PLoS ONE. 10(8). e0135555–e0135555. 41 indexed citations

5.

Coppola, Antonietta, Antonio Romito, Christelle Borel, et al.. (2013). Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications. Stem Cell Research. 12(2). 323–337. 59 indexed citations

6.

Nikolaev, Sergey I., Donata Rimoldi, Christian Iseli, et al.. (2011). Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma. Nature Genetics. 44(2). 133–139. 295 indexed citations

7.

Borel, Christelle, Samuel Deutsch, Audrey Letourneau, et al.. (2010). Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts. Genome Research. 21(1). 68–73. 52 indexed citations

8.

Moldrich, Randal X., Luce Dauphinot, Julien Laffaire, et al.. (2009). Proliferation deficits and gene expression dysregulation in Down's syndrome (Ts1Cje) neural progenitor cells cultured from neurospheres. Journal of Neuroscience Research. 87(14). 3143–3152. 35 indexed citations

9.

Prandini, Paola, Samuel Deutsch, Robert Lyle, et al.. (2007). Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance. The American Journal of Human Genetics. 81(2). 252–263. 145 indexed citations

10.

Lyle, Robert, Uppala Radhakrishna, Jean‐Louis Blouin, et al.. (2006). Split‐hand/split‐foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region. American Journal of Medical Genetics Part A. 140A(13). 1384–1395. 27 indexed citations

11.

Deutsch, Samuel, Robert Lyle, Emmanouil T. Dermitzakis, et al.. (2005). Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes. Human Molecular Genetics. 14(23). 3741–3749. 89 indexed citations

12.

Lyle, Robert, et al.. (2004). Gene Expression From the Aneuploid Chromosome in a Trisomy Mouse Model of Down Syndrome. Genome Research. 14(7). 1268–1274. 160 indexed citations

13.

Brandt-Casadevall, C., M. Gené, Ester Piqué, et al.. (2003). Presence of two mutations between father and child in two cases of paternity testing. International Congress Series. 1239. S15–S18. 5 indexed citations

14.

Gehrig, Corinne, M Armengot, M Rutishauser, et al.. (2002). DNAH3: Characterization of the sequence and mutation search in patients with Primary Ciliary Dyskinesia. European Journal of Human Genetics. 10. 138. 5 indexed citations

15.

Bartoloni, Lucia, Jean‐Louis Blouin, Yanzhen Pan, et al.. (2002). Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia. Proceedings of the National Academy of Sciences. 99(16). 10282–10286. 233 indexed citations

16.

Bartoloni, Lucia, Jean‐Louis Blouin, Amit K. Maiti, et al.. (2001). Axonemal Beta Heavy Chain Dynein DNAH9: cDNA Sequence, Genomic Structure, and Investigation of Its Role in Primary Ciliary Dyskinesia. Genomics. 72(1). 21–33. 39 indexed citations

17.

Radhakrishna, Uppala, Selahattin Şenol, Hasan Herken, et al.. (2001). An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2–q11.2 in a large Turkish pedigree. European Journal of Human Genetics. 9(1). 39–44. 30 indexed citations

18.

Maiti, Amit K., Lucia Bartoloni, Hannah M. Mitchison, et al.. (2000). No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD). Cytogenetic and Genome Research. 90(1-2). 119–122. 27 indexed citations

19.

Antonarakis, Stylianos E., Jean‐Louis Blouin, Virginia K. Lasseter, et al.. (1999). Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21. American Journal of Medical Genetics. 88(4). 348–351. 30 indexed citations

20.

Antonarakis, Stylianos E., Jean‐Louis Blouin, Virginia K. Lasseter, et al.. (1999). Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21. American Journal of Medical Genetics. 88(4). 348–351. 2 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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