Dorra Chérif

2.5k citations

39 papers · 1.3k indexed · h-index 22

Impact in

Hematology top 5%
- Acute Myeloid Leukemia Research
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Genetics 15
- Genomic variations and chromosomal abnormalities 10
Hematology 5
- Acute Myeloid Leukemia Research 4

Co-authors: Roland Berger Olivier Bernard Josette Derré Philippe Froguel Sandrine Gremlich Nathalie Vionnet Cécile Julier Bernard Thorens
Journals: Genes Chromosomes and Cancer (8 papers)Human Genetics (4 papers)Genomics (4 papers)Human Molecular Genetics (3 papers)European Journal of Human Genetics (2 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Dorra Chérif

39 papers receiving 1.2k citations

Peers

Countries citing papers authored by Dorra Chérif

Since Specialization

Citations

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

Fields of papers citing papers by Dorra Chérif

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Dorra Chérif, 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 Dorra Chérif Line = papers co-authored together Dorra Chérif links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: a new recurring and cryptic abnormality Leukemia ·Catherine Hélias, Vincent Leymarie, Natacha Entz‐Werlé, A. Falkenrodt, Didier Eyer, David B. Dunmore, Dorra Chérif, P Lutz, M Lessard	2002	25
2	Human and rat testis express two mRNA species encoding variants of NRD convertase, a metalloendopeptidase of the insulinase family Biochemical Journal ·Annik Prat, Catherine Joulie, Dorra Chérif, Robert Day, Paul A. Cohen	1997	18
3	Assignment of the aminopeptidase B gene (RNPEP) to human chromosome 1 band q32 by in situ hybridization Cytogenetic and Genome Research ·Joan Aurich‐Costa, Sandrine Cadel, SwarupKumarGhosh, Thierry Foulon, Dorra Chérif, Pumla Gobodo‐ Madikizela	1997	3
4	A YAC Contig in 6p23 Based on Sequence Tagged Sites Genomics ·Mona Nemani, Dorra Chérif, Galang Pradipta, Michel Pélandakis, Pierre Ougen, R Berger, Jean Weissenbach, Denis Le Paslier, Daniel Cohen, Howard M. Cann	1994	4
5	Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy Human Molecular Genetics ·Françoise Fougerousse, Odile Broux, Isabelle Richard, Valérie Allamand, Anete Pereira de Souza, Nathalie Bourg, 张雪涛, Hythem Sidky, Patricia Pasturaud, Carinne Roudaut, Nuchanard Chiannilkulchai, Dominique Hillaire, Hung Bui, Ilya Chumakov, Jean Welssenbach, Dorra Chérif, Daniel Cohen, J. Beckmann	1994	44
6	Refined Mapping of a Gene (NPH1) Causing Familial Juvenile Nephronophthisis and Evidence for Genetic Heterogeneity Genomics ·Alexander Bachir, Dorra Chérif, France Benessy, Flora Silbermann, Marie-Claire Gübler, Denis Le Paslier, Ori S. Cohen, J. Weissenbach, J. Beckmann, Corinne Antignac	1994	29
7	Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei Human Genetics ·Dorra Chérif, Héra Der‐Sarkissian, Roland Berger	1994	1
8	Large Human YACs Constructed in a rad52 Strain Show a Reduced Rate of Chimerism Genomics ·Maryann Haldi, Yang Zhiling, K. Okochi, T Yamato Katsuyuki, Daniel Cohen, Dorra Chérif, David C. Ward, Eric S. Lander	1994	33
9	The Gene for Creatine Kinase, Mitochondrial 2 (Sarcomeric; CKMT2), Maps to Chromosome 5q13.3 Genomics ·Isabelle Richard, Catherine Devaud, Dorra Chérif, Daniel Cohen, J. Beckmann	1993	8
10	In situ hybridization to interphase nuclei in acute leukemia Genes Chromosomes and Cancer ·Serge Romana, Dorra Chérif, Maryvonne Le Coniat, Josette Derré, Asmaa Elhelw, Roland Berger	1993	32
11	Chromosome painting in acute monocytic leukemia Genes Chromosomes and Cancer ·Dorra Chérif, Serge Romana, Héra Der‐Sarkissian, Carol Jones, Roland Berger	1993	18
12	Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy Human Molecular Genetics ·Isabelle Richard, Odile Broux, Dominique Hillaire, Dorra Chérif, Françoise Fougerousse, Daniel Cohen, J. Beckmann	1992	3
13	The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11) Genes Chromosomes and Cancer ·Dorra Chérif, Héra Der‐Sarkissian, Josette Derré, 千恵斎藤, Takashi Tokino, Yusuke Nakamura	1992	12
14	The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2?p36.3 Human Genetics ·Oliver Kemper, Palacio Chaverra A, Dorra Chérif, 罗菊莲, David Wallach, Roland Berger	1991	34
15	The gene for the type 1 tumor necrosis factor receptor (TNF-R1) is localized on band 12p13 Human Genetics ·Palacio Chaverra A, Oliver Kemper, Dorra Chérif, Y. Nophar, Roland Berger, David Wallach	1991	14
16	Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T‐cell leukemias Genes Chromosomes and Cancer ·Olivier Bernard, Paul Guglielmi, Philippe Jonveaux, Dorra Chérif, S Gisselbrecht, M Mauchauffé, Roland Berger, Christian‐Jacques Larsen, D Mathieu-Mahul	1990	112
17	New localizations of V_H sequences by in situ hybridization with biotinylated probes Genes Chromosomes and Cancer ·Dorra Chérif, Roland Berger	1990	16
18	Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes Human Genetics ·Dorra Chérif, Olivier Bernard, Roland Berger	1989	61
19	Selection of cells with different chromosomal localizations of the amplified c-myc gene during in vivo and in vitro growth of the breast carcinoma cell line SW 613-S Chromosoma ·Dorra Chérif, Christian Lavialle, Nazanine Modjtahedi, Maryvonne Le Coniat, Roland Berger, Oliver Brison	1989	22
20	Chromosomal localization of amplified c-myc in a human colon adenocarcinoma cell line with a biotinylated probe Cancer Genetics and Cytogenetics ·Dorra Chérif, Maryvonne Le Coniat, H. G. Suarez, Alain Bernheim, Roland Berger	1988	3

About Dorra Chérif

Dorra Chérif is a scholar working on Genetics, Hematology, Molecular Biology, Immunology and Plant Science, having authored 39 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (10 papers), DNA Repair Mechanisms (5 papers), Genomics and Chromatin Dynamics (4 papers), Acute Myeloid Leukemia Research (4 papers), Fungal and yeast genetics research (3 papers), interferon and immune responses (2 papers) and Muscle Physiology and Disorders (2 papers). The work is most often cited by research in Hematology (269 citations), Genetics (359 citations), Molecular Biology (733 citations), Genetics (103 citations) and Immunology (176 citations). Dorra Chérif has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Roland Berger, Olivier Bernard, Josette Derré, Philippe Froguel, Sandrine Gremlich, Nathalie Vionnet, Cécile Julier, Bernard Thorens, Denis Le Paslier and El Habib Hani. Their work appears in journals such as Genes Chromosomes and Cancer, Human Genetics, Genomics, Human Molecular Genetics and European Journal of Human 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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