Boris Keren

13.4k citations

70 papers · 1.1k indexed · h-index 21

Impact in

Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Molecular Biology
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Protein Tyrosine Phosphatases

Papers in

Genetics 42
- Genetics and Neurodevelopmental Disorders 19
- Genomics and Rare Diseases 17
- Genomic variations and chromosomal abnormalities 13
- Genetic Syndromes and Imprinting 10
Molecular Biology 45
- RNA modifications and cancer 10
- Epigenetics and DNA Methylation 9

Co-authors: Sandra Chantot‐Bastaraud Alain Verloès Christel Depienne Jean‐Pierre Siffroi Cyril Mignot Salah Azzi Irène Netchine Alexis Brice
Journals: European Journal of Medical Genetics (9 papers)Journal of Medical Genetics (5 papers)European Journal of Paediatric Neurology (4 papers)Human Mutation (4 papers)Clinical Genetics (3 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Boris Keren

67 papers receiving 1.0k citations

Peers

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

The 25 scholars most cited alongside Boris Keren, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Boris Keren Line = papers co-authored together Boris Keren links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up Prenatal Diagnosis ·Jurgen Heinz Schawacht, Stéphanie Valence, Saskia Vande Perre, Ferdinand Dhombres, Delphine Héron, Thierry Billette de Villemeur, Boris Keren, Alexandra Afenjar, F. v. Kobell, 廖清高, T Watabe, Diana Rodriguez, Jean‐Marie Jouannic, Lydie Bürglen, Cathérine Garel	2024	1
2	Expanding MNS1 Heterotaxy Phenotype American Journal of Medical Genetics Part A ·T Girolamo, Andrée Delahaye‐Duriez, Hui Duan, Ange‐Line Bruel, Anne‐Sophie Denommé‐Pichon, Alexander Iosad, Christel Thauvin‐Robinet, 文哉吉永, Véronique Satre, Dana Idrissova, Donald W. Codding, Boris Keren, Laurence Faivre	2024	1
3	Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder Pediatric Neurology ·Weller Ac, Chenxiang Qian, Siddharth Srivastava, Lindsay C. Swanson, Boris Keren, Sandra Whalen, Cyril Mignot, Magdalena Vähäkangas, Qian Chen, Jill A. Rosenfeld, Scott McLean, Rebecca O. Littlejohn, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Sureni V. Mullegama, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2024	0
4	A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report Acta Neuropathologica Communications ·Veena Raparthi, Boris Keren, Cyril Mignot, Richard S. Brush, Marie‐Cécile Nassogne, Martin‐Paul Agbaga	2023	3
5	Unexpected Inheritance Patterns in a Large Cohort of Patients with a Suspected Ciliopathy Human Mutation ·真顕三上, Harbal S Bijral, A. Cervantes-Tobón, Melissa A. Morgunov, Sylvie Friedmann, Joseph Mutch, Lv Pan, Christine Francannet, Boris Keren, Jonathan Lévy, Rexiati Keranmu, Qian Cheng, Jeanne Amiel, Hélène Dollfus, Sophie Scheidecker, Jean Muller	2023	0
6	Deep Characterization of a Greek Patient with Desmin-Related Myofibrillar Myopathy and Cardiomyopathy International Journal of Molecular Sciences ·Constantinos Papadopoulos, Edoardo Malfatti, Corinne Métay, Boris Keren, محمد الهادی, Julien Buratti, Sophia Xirou, Aswad Eka Putra, George K. Papadimas	2023	2
7	Spectrum of brain malformations in fetuses with mild tubulinopathy Ultrasound in Obstetrics and Gynecology ·David W. Perrin, Karina Krajden Haratz, G. Malinger, Liat Ben‐Sira, Z. Leibovitz, Delphine Héron, Lydie Bürglen, R. Birnbaum, 林瑛, Boris Keren, 田辺健一郎, Jean‐Marie Jouannic, Tally Lerman‐Sagie, Cathérine Garel	2022	10
8	Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders Clinical Genetics ·Nguyen Van Thoan, BI Yao-bai, Bitten Schönewolf‐Greulich, Alexandra Afenjar, Magalie Barth, Felix Boschann, Diane Doummar, Tobias B. Haack, Boris Keren, Л. А. Лившиц, Davide Mei, Joohyun Park, Tiziana Pisano, Luis Anglada, Muhammad Umair, Ahmed Waqas, Alban Ziegler, Renzo Guerrini, Rikke S. Møller, Zeynep Tümer	2021	26
9	Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome Journal of Medical Genetics ·Е В Сократова, Olivier Patat, Sandra Whalen, Lionel Arnaud, Giulia Barcia, Julien Buratti, Benjamin Cogné, Diane Doummar, Rustamova Z. Sh., И. М. Назаркина, Éric Leguern, Gaëtan Lesca, Caroline Nava, Mathilde Nizon, Amélie Piton, Stéphanie Valence, Laurent Villard, Sarah Weckhuysen, Boris Keren, Cyril Mignot	2021	8
10	Tremor-like subcortical myoclonus in STXBP1 encephalopathy European Journal of Paediatric Neurology ·M.C. Gobbi, Diane Doummar, Amador Vega Esquerra, Thierry Bienvenu, Perrine Charles, Christel Depienne, Nathalie Dorison, Solveig Heide, Delphine Héron, Christine Ioos, Boris Keren, J.A Macias-masas, Fanny Mochel, Marie‐Laure Moutard, Claudia Ravelli, Emmanuelle Apartis, Cyril Mignot	2021	4
11	Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males Human Genetics ·Hans‐Jürgen Kreienkamp, Matias Wagner, Heike Weigand, 兼原壽生, Marie McDonald, Boris Keren, Cyril Mignot, Julie Gauthier, Mohamed Sahr Lebbie, Jacques L. Michaud, Shaibatul ’ Islamiah Che Man, Rosemarie Smith, Ulrike Löbel, Maja Hempel, Christian Kubisch, Jonas Denecke, Philippe M. Campeau, Jennifer Bain, Davor Lessel	2021	13
12	Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic Paraplegia Neurology Genetics ·苏艳秋, Boris Keren, Íñigo Marcos‐Alcalde, Paulino Gómez‐Puertas, Fanny Mochel, Pedro A. Lazo	2021	5
13	Loss‐of‐function variants in ARHGEF9 are associated with an X‐linked intellectual disability dominant disorder Human Mutation ·Katsuhiko KASHIBA, Thomas Besnard, Mathilde Nizon, Shugo Sakaguchi, MW van Eekelen, Shuanglin Luo, Christel Thauvin‐Robinet, Ange‐Line Bruel, Paul Kuentz, Christine Coubes, Laurence Cuisset, Cyril Mignot, Boris Keren, Stéphane Bezieau, Benjamin Cogné	2021	2
14	Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings American Journal of Medical Genetics Part A ·Maud Blanluet, Sandra Chantot‐Bastaraud, Pascal Chambon, Kévin Cassinari, Gabriella Vera, Alice Goldenberg, Boris Keren, Nathalie Le Meur, Didier Hannequin, Bertrand Macé, Jean‐Pierre Siffroi, Thierry Frébourg, Gaël Nicolas, Géraldine Joly‐Hélas	2021	1
15	New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability Clinical Genetics ·Lise Larcher, Julien Buratti, A. I. Bartyzel', Brigitte Benzacken, Eva Pipiras, Boris Keren, Andrée Delahaye‐Duriez	2019	7
16	The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndrome European Journal of Medical Genetics ·Lise Larcher, Joy Norris, محمد الهادی, Julien Buratti, Cyril Mignot, Cathérine Garel, Boris Keren, Charles E. Schwartz, Sandra Whalen	2019	21
17	NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder Clinical Genetics ·Jonathan Lévy, Sarah Grotto, Cyril Mignot, A. Maruani, Andrée Delahaye‐Duriez, Brigitte Benzacken, Boris Keren, Damien Haye, Sarah J. Court, Mar Cusó Banús, Anna Rickardsson, Alain Verloès, Céline Dupont, Eva Pipiras, Anne‐Claude Tabet	2018	25
18	Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences Journal of Medical Genetics ·Solveig Heide, Sandra Chantot‐Bastaraud, Boris Keren, Madeleine D. Harbison, Salah Azzi, Sylvie Rossignol, Caroline Michot, Onnalin Mancaket, Bénédicte Demeer, Claudine Heinrichs, Ron S. Newfield, Pierre Sarda, Lionel Van Maldergem, Lubka Marinova, Éloïse Giabicani, Jean‐Pierre Siffroi, Yves Le Bouc, Irène Netchine, Frédéric Brioude	2017	34
19	Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome Human Molecular Genetics ·Walid Abi Habib, Salah Azzi, Frédéric Brioude, Virginie Steunou, Nathalie Thibaud, Wenzhu Huang Wenzhu Huang, Paras Subodh Karpe, Sandra Chantot‐Bastaraud, Boris Keren, Stanislas Lyonnet, Caroline Michot, Massimiliano Rossi, Laurent Pasquier, Christine Gicquel, Sylvie Rossignol, Yves Le Bouc, Irène Netchine	2014	51
20	Biotin-Responsive Basal Ganglia Disease in Ethnic Europeans With Novel SLC19A3 Mutations Archives of Neurology ·Rabab Debs, Christel Depienne, Agnès Rastetter, Agnès Bellanger, Bertrand Degos, Damien Galanaud, Boris Keren, O. Lyon‐Caen, Alexis Brice, Frédéric Sedel	2010	73

About Boris Keren

Boris Keren is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Cell Biology, having authored 70 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (19 papers), Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (13 papers), Genetic Syndromes and Imprinting (10 papers), Prenatal Screening and Diagnostics (10 papers), RNA modifications and cancer (10 papers), Epigenetics and DNA Methylation (9 papers) and Genetic Neurodegenerative Diseases (5 papers). The work is most often cited by research in Genetics (515 citations), Molecular Biology (649 citations), Pediatrics, Perinatology and Child Health (154 citations), Clinical Biochemistry (49 citations) and Neurology (105 citations). Boris Keren has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Sandra Chantot‐Bastaraud, Alain Verloès, Christel Depienne, Jean‐Pierre Siffroi, Cyril Mignot, Salah Azzi, Irène Netchine, Alexis Brice, Sylvie Rossignol and Frédéric Brioude. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, European Journal of Paediatric Neurology, Human Mutation and Clinical Genetics.

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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