Sabine Quief

2.2k total citations
29 papers, 1.8k citations indexed

About

Sabine Quief is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Sabine Quief has authored 29 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Pathology and Forensic Medicine and 7 papers in Genetics. Recurrent topics in Sabine Quief's work include Cancer-related gene regulation (11 papers), Lymphoma Diagnosis and Treatment (10 papers) and Acute Myeloid Leukemia Research (7 papers). Sabine Quief is often cited by papers focused on Cancer-related gene regulation (11 papers), Lymphoma Diagnosis and Treatment (10 papers) and Acute Myeloid Leukemia Research (7 papers). Sabine Quief collaborates with scholars based in France, United Kingdom and United States. Sabine Quief's co-authors include Jean‐Pierre Kerckaert, Clotilde Deweindt, Olivier Albagli, Christian Bastard, Philippe Dhordain, Hervé Tilly, Danièle Lantoine, Dominique Leprince, Richard J. Lin and Ronald M. Evans and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Sabine Quief

29 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sabine Quief France 19 944 520 472 401 395 29 1.8k
Clotilde Deweindt France 8 715 0.8× 549 1.1× 334 0.7× 376 0.9× 378 1.0× 8 1.4k
Kenneth Nakahara United States 12 798 0.8× 361 0.7× 316 0.7× 385 1.0× 264 0.7× 15 1.6k
P Goldman United States 11 1.2k 1.2× 713 1.4× 679 1.4× 658 1.6× 571 1.4× 11 2.3k
Florence Ajchenbaum‐Cymbalista France 23 550 0.6× 670 1.3× 612 1.3× 575 1.4× 909 2.3× 40 1.7k
Marie Lia United States 11 1.3k 1.3× 508 1.0× 642 1.4× 413 1.0× 303 0.8× 17 2.2k
Paul D. Sherrington United Kingdom 21 1.1k 1.1× 460 0.9× 541 1.1× 578 1.4× 714 1.8× 40 2.1k
Katerina Hatzi United States 24 1.1k 1.2× 711 1.4× 1.1k 2.3× 500 1.2× 758 1.9× 46 2.5k
Blanca Scheijen Netherlands 24 1.5k 1.6× 374 0.7× 311 0.7× 615 1.5× 282 0.7× 53 2.6k
Naoki Kakazu Japan 17 852 0.9× 140 0.3× 335 0.7× 265 0.7× 190 0.5× 40 1.5k
P C Nowell United States 18 630 0.7× 167 0.3× 363 0.8× 240 0.6× 203 0.5× 26 1.2k

Countries citing papers authored by Sabine Quief

Since Specialization
Citations

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

Fields of papers citing papers by Sabine Quief

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Quief

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

All Works

20 of 20 papers shown
1.
Salson, Mikaël, Mathieu Giraud, Aurélie Caillault, et al.. (2016). High-throughput sequencing in acute lymphoblastic leukemia: Follow-up of minimal residual disease and emergence of new clones. Leukemia Research. 53. 1–7. 14 indexed citations
2.
Giraud, Mathieu, Mikaël Salson, Céline Villenet, et al.. (2014). Fast multiclonal clusterization of V(D)J recombinations from high-throughput sequencing. BMC Genomics. 15(1). 409–409. 47 indexed citations
3.
Marceau‐Renaut, Alice, Aline Renneville, Olivier Nibourel, et al.. (2013). New-generation sequencing (NGS) in hematologic oncology laboratories. Hématologie. 19(2). 112–122. 2 indexed citations
4.
Leprêtre, Frédéric, Céline Villenet, Sabine Quief, et al.. (2010). Waved aCGH: to smooth or not to smooth. Nucleic Acids Research. 38(7). e94–e94. 18 indexed citations
5.
Ruminy, Philippe, Jean Pierre Kerckaert, F Parmentier, et al.. (2008). Detection of somatic quantitative genetic alterations by multiplex polymerase chain reaction for the prediction of outcome in diffuse large B-cell lymphomas. Haematologica. 93(4). 543–550. 23 indexed citations
6.
7.
Leroy, Catherine, Julien Deheuninck, Sylvie Reveneau, et al.. (2006). HGF/SF Regulates Expression of Apoptotic Genes in MCF‐10A Human Mammary Epithelial Cells. Annals of the New York Academy of Sciences. 1090(1). 188–202. 6 indexed citations
8.
Andrieux, Joris, Jean‐Loup Demory, Brigitte Dupriez, et al.. (2003). Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia. Genes Chromosomes and Cancer. 39(1). 82–87. 39 indexed citations
9.
Albagli, Olivier, Catherine Lindon, Danièle Lantoine, et al.. (2000). DNA Replication Progresses on the Periphery of Nuclear Aggregates Formed by the BCL6 Transcription Factor. Molecular and Cellular Biology. 20(22). 8560–8570. 15 indexed citations
10.
Albagli, Olivier, Danièle Lantoine, Sabine Quief, et al.. (1999). Overexpressed BCL6 (LAZ3) oncoprotein triggers apoptosis, delays S phase progression and associates with replication foci. Oncogene. 18(36). 5063–5075. 59 indexed citations
11.
Galiègue‐Zouitina, Sylvie, Sabine Quief, Marie‐Paule Hildebrand, et al.. (1999). Nonrandom fusion of LPlastinLCP1 and LAZ3BCL6 genes by t(3;13)(q27;q14) chromosome translocation in two cases of B‐cell non‐Hodgkin lymphoma. Genes Chromosomes and Cancer. 26(2). 97–105. 3 indexed citations
12.
Dhordain, Philippe, Sabine Quief, Danièle Lantoine, et al.. (1998). The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression. Nucleic Acids Research. 26(20). 4645–4651. 202 indexed citations
13.
Albagli, Olivier, Philippe Dhordain, Danièle Lantoine, et al.. (1998). Increased expression of the LAZ3 (BCL6) proto-oncogene accompanies murine skeletal myogenesis. Differentiation. 64(1). 33–44. 21 indexed citations
14.
15.
Quief, Sabine, et al.. (1996). Molecular cloning and structural analysis of cDNAs that encode 3 small GTP-binding proteins from sugar beet.. PubMed. 319(2). 91–7. 4 indexed citations
16.
Albagli, Olivier, et al.. (1996). Multiple Domains Participate in Distance-Independent LAZ3/BCL6-Mediated Transcriptional Repression. Biochemical and Biophysical Research Communications. 220(3). 911–915. 42 indexed citations
17.
Dhordain, Philippe, Olivier Albagli, Stéphane Ansieau, et al.. (1995). The BTB/POZ domain targets the LAZ3/BCL6 oncoprotein to nuclear dots and mediates homomerisation in vivo.. PubMed. 11(12). 2689–97. 102 indexed citations
18.
Deweindt, Clotilde, Jean‐Pierre Kerckaert, Hervé Tilly, et al.. (1993). Cloning of a breakpoint cluster region at band 3q27 involved in human non‐Hodgkin's lymphoma. Genes Chromosomes and Cancer. 8(3). 149–154. 61 indexed citations
19.
Kerckaert, Jean‐Pierre, et al.. (1993). LAZ3, a novel zinc–finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomas. Nature Genetics. 5(1). 66–70. 376 indexed citations
20.
Galiègue‐Zouitina, Sylvie, et al.. (1993). Quantitative and qualitative variation of ETS-1 transcripts in hematologic malignancies.. PubMed. 7(11). 1777–85. 12 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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