Boris Keren

879 total citations
10 papers, 235 citations indexed

About

Boris Keren is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Boris Keren has authored 10 papers receiving a total of 235 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Boris Keren's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Boris Keren is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Boris Keren collaborates with scholars based in France, United States and Germany. Boris Keren's co-authors include Nadia Bahi‐Buisson, Isabelle Desguerre, David Geneviève, Nathalie Boddaert, Jamel Chelly, Catherine Fallet‐Bianco, Férechté Encha‐Razavi, Christine Barnérias, Yoann Saillour and Nicolas Lebrun and has published in prestigious journals such as Human Molecular Genetics, Epilepsia and Frontiers in Physiology.

In The Last Decade

Boris Keren

5 papers receiving 230 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Boris Keren France	4	141	110	64	40	38	10	235
Başak Rosti United States	5	126 0.9×	71 0.6×	59 0.9×	40 1.0×	39 1.0×	8	204
Stéphanie Valence France	11	217 1.5×	158 1.4×	114 1.8×	123 3.1×	64 1.7×	22	407
Antonella Sferra Italy	8	151 1.1×	78 0.7×	43 0.7×	11 0.3×	47 1.2×	12	246
Sue Kenwrick United Kingdom	10	203 1.4×	65 0.6×	114 1.8×	29 0.7×	95 2.5×	11	335
Keri Ramsey United States	10	163 1.2×	54 0.5×	97 1.5×	18 0.5×	27 0.7×	14	255
Loïc Broix Belgium	8	165 1.2×	88 0.8×	58 0.9×	15 0.4×	43 1.1×	11	253
Carissa Adams United States	2	171 1.2×	39 0.4×	124 1.9×	32 0.8×	29 0.8×	3	275
Eric Scott United States	6	128 0.9×	76 0.7×	55 0.9×	15 0.4×	24 0.6×	8	194
Sébastien Moutton France	12	212 1.5×	45 0.4×	211 3.3×	33 0.8×	64 1.7×	17	367
Julian Curiel United States	7	202 1.4×	96 0.9×	34 0.5×	8 0.2×	46 1.2×	9	305

Countries citing papers authored by Boris Keren

Since Specialization

Citations

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

Fields of papers citing papers by Boris Keren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Boris Keren

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

Chiţimuș, Diana Maria, Clovis Adam, Cécile Cauquil, et al.. (2025). Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure. Revue Neurologique. 181(8). 759–764.

Aupy, Jérôme, Laurent Villard, Nathalie Villeneuve, et al.. (2025). GABRA2‐related encephalopathy: Identification of two phenotypes with distinctive electroclinical features. Epilepsia. 66(8).

Huang, Alden, et al.. (2024). Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genetics in Medicine. 26(11). 101218–101218.

Zaki, Maha S., Mahmoud Y. Issa, Boris Keren, et al.. (2024). Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesis. Human Genetics. 143(11). 1353–1362. 1 indexed citations

Gorokhova, Svetlana, Cécile Rouzier, Cécile Acquaviva, et al.. (2024). Interprétation des résultats issus du séquençage à haut débit pour les maladies génétiques. médecine/sciences. 40(10). 767–769.

Lipska‐Ziętkiewicz, Beata S., Vincent Michaud, James Lespinasse, et al.. (2022). Phenotypic characterization of seven individuals with Marbach–Schaaf neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 188(9). 2627–2636. 3 indexed citations

Hiatt, Susan M., Sandra Whalen, Boris Keren, et al.. (2019). A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK Pathway. Frontiers in Physiology. 10. 388–388. 25 indexed citations

Keren, Boris & Cédric Le Caignec. (2011). Oligonucleotide microarrays in constitutional genetic diagnosis. Expert Review of Molecular Diagnostics. 11(5). 521–532. 12 indexed citations

Poirier, Karine, Yoann Saillour, Nadia Bahi‐Buisson, et al.. (2010). Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects. Human Molecular Genetics. 19(22). 4462–4473. 194 indexed citations

10.

Keren, Boris & Damien Sanlaville. (2008). Nouveaux outils diagnostiques du retard mental. MTP. Médecine thérapeutique pédiatrie. 11(4). 230–241.

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.

Explore authors with similar magnitude of impact