Faouzi Baklouti

1.2k citations

66 papers · 971 indexed · h-index 19

Physiology top 5%
Molecular Biology
Pulmonary and Respiratory Medicine top 10%
Genetics top 5%
Hematology top 5%

Co-authors: J. Delaunay Laurette Morlé Nicole Alloisio Madeleine Morinière J Maréchal Philippe Maillet R Kastally R Wilmotte
Topics: Erythrocyte Function and Pathophysiology (37 papers)RNA Research and Splicing (18 papers)RNA modifications and cancer (16 papers)
Cited by: Genetics Physiology Hematology
Journals: Journal of Clinical Investigation Blood PLoS ONE
Partner nations: France United States Tunisia

In The Last Decade

Faouzi Baklouti

65 papers receiving 964 citations

Peers

Countries citing papers authored by Faouzi Baklouti

Since Specialization

Citations

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

Fields of papers citing papers by Faouzi Baklouti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Faouzi Baklouti

This figure shows the co-authorship network connecting the top 25 collaborators of Faouzi Baklouti. A scholar is included among the top collaborators of Faouzi Baklouti 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 Faouzi Baklouti. Faouzi Baklouti 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

#	Work	Indexed citations
1	SMA-linked SMN mutants prevent phase separation properties and SMN interactions with FMRP family members 2022 ·Life Science Alliance ·Olivier Binda,Franceline Juillard,(unknown),(unknown),Geneviève Paris,(unknown),Faouzi Baklouti,Armelle Corpet,Yohann Couté,Jocelyn Côté,Patrick Lomonte	7
2	JAK2V617F mRNA metabolism in myeloproliferative neoplasm cell lines 2014 ·Blood Cancer Journal ·Pauline Nauroy,François Delhommeau,Faouzi Baklouti	4
3	Proteasome-Mediated Proteolysis of SRSF5 Splicing Factor Intriguingly Co-occurs with SRSF5 mRNA Upregulation during Late Erythroid Differentiation 2013 ·PLoS ONE ·(unknown),Faouzi Baklouti	18
4	Combined inhibition of PI3K and activation of MAPK p38 signaling pathways trigger erythroid alternative splicing switch of 4.1R pre-mRNA in DMSO-induced erythroleukemia cells 2013 ·Cellular Signalling ·(unknown),(unknown),Faouzi Baklouti	6
5	Subtle distinct regulations of late erythroid molecular events by PI3K/AKT-mediated activation of Spi-1/PU.1 oncogene autoregulation loop 2010 ·Oncogene ·(unknown),(unknown),(unknown),Faouzi Baklouti	16
6	Subtle discrepancies of SF2/ASF ESE sequence motif among human tissues: A computational approach 2010 ·Computational Biology and Chemistry ·(unknown),Ahmed Rebaï,Faouzi Baklouti,Faiza Fakhfakh	1
7	Nonsense-mediated mRNA decay (NMD) blockage promotes nonsense mRNA stabilization in protein 4.1R deficient cells carrying the 4.1R Coimbra variant of hereditary elliptocytosis 2010 ·Blood Cells Molecules and Diseases ·Madeleine Morinière,François Delhommeau,Alain Calender,Letícia Ribeiro,J. Delaunay,Faouzi Baklouti	7
8	Downregulation of the Spi-1/PU.1 oncogene induces the expression of TRIM10/HERF1, a key factor required for terminal erythroid cell differentiation and survival 2008 ·Cell Research ·(unknown),(unknown),(unknown),Faouzi Baklouti	26
9	Severe MDC1A Congenital Muscular Dystrophy Due to a Splicing Mutation in the LAMA2 Gene Resulting in Exon Skipping and Significant Decrease of mRNA Level 2007 ·Genetic Testing ·(unknown),(unknown),Chahnez Triki,Madeleine Morinière,Ahmed Rebaï,Pascale Richard,Pascale Guicheney,Faouzi Baklouti,Faiza Fakhfakh	11
10	Des oncogènes à l’interface entre transcription et épissage 2004 ·médecine/sciences ·(unknown),Faouzi Baklouti	1
11	Spi-1/PU.1 but not Fli-1 inhibits erythroid-specific alternative splicing of 4.1R pre-mRNA in murine erythroleukemia cells 2003 ·Oncogene ·(unknown),(unknown),Madeleine Morinière,Joëlle Starck,Françoise Moreau-Gachelin,François Morlé,Faouzi Baklouti	11
12	A missense mutation (Q279R) in the Fumarylacetoacetate Hydrolase gene, responsible for hereditary tyrosinemia, acts as a splicing mutation 2001 ·BMC Genetics ·Natacha Dreumont,(unknown),Anne Bergeron,Harvey L. Levy,Faouzi Baklouti,Robert M. Tanguay	20
13	A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon 1999 ·Human Mutation ·Philippe Maillet,Nicole Dalla Venezia,(unknown),(unknown),Muriel Bozon,(unknown),J. Delaunay,Faouzi Baklouti	9
14	Stop codon in exon 30 (E2069X) of β-spectrin gene associated with hereditary elliptocytosis in spectrin Nagoya 1996 ·Human Mutation ·Philippe Maillet,Takafumi Inoue,Akio Kanzaki,Ayumi Yawata,Koji Kato,Faouzi Baklouti,J. Delaunay,Yoshihito Yawata	7
15	Band 3 Chur: a variant associated with band 3‐deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11 1995 ·British Journal of Haematology ·Philippe Maillet,Agnès Vallier,Walter H. Reinhart,(unknown),Peter Ott,Pascale Texier,Faouzi Baklouti,M J A Tanner,J. Delaunay,Nicole Alloisio	30
16	Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton. 1994 ·Journal of Clinical Investigation ·Felipe Lorenzo,Nicole Dalla Venezia,Laurette Morlé,Faouzi Baklouti,Nicole Alloisio,(unknown),(unknown),(unknown),J. Delaunay	29
17	Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46. 1993 ·Journal of Clinical Investigation ·R Wilmotte,J Maréchal,Laurette Morlé,Faouzi Baklouti,N Philippe,R Kastally,Leszek Kotula,J. Delaunay,Nicole Alloisio	80
18	Open‐heart surgery in a patient with a high oxygen affinity haemoglobin variant 1989 ·Anaesthesia ·Alain Francina,D. Chassard,Faouzi Baklouti,Matthieu George,S Estanove	3
19	δ°‐Thalassemia in cis of β^Knossos‐globin gene Normal structure and normal transient expression of the δ‐globin gene 1989 ·FEBS Letters ·(unknown),Dominique Bozon,Faouzi Baklouti,C. Gonnet,J. Delaunay,Jacqueline Godet	3
20	Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O‐Arab (β121[GH4]Glu→Lys) in a Moroccan man 1988 ·American Journal of Hematology ·Faouzi Baklouti,Alain Francina,(unknown),(unknown),(unknown),Henri Plauchu,Henri Wajcman,J. Delaunay,Jacqueline Godet	2

About Faouzi Baklouti

Faouzi Baklouti is a scholar working on Genetics, Hematology and Physiology, having authored 66 papers that have together received 971 indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (37 papers), RNA Research and Splicing (18 papers) and RNA modifications and cancer (16 papers). The work is most often cited by research in Genetics (234 citations), Physiology (536 citations) and Hematology (198 citations). Faouzi Baklouti has collaborated with scholars based in France, United States and Tunisia. Frequent co-authors include J. Delaunay, Laurette Morlé, Nicole Alloisio, Madeleine Morinière, J Maréchal, Philippe Maillet, R Kastally, R Wilmotte, Shu‐Ching Huang and Edward J. Benz. Their work appears in journals such as Journal of Clinical Investigation, Blood and PLoS ONE.

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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