Nizar Smaoui

7.6k citations

29 papers · 938 indexed · h-index 17

Ophthalmology top 2%
Genetics top 5%
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 2
Molecular Biology top 10%
- Retinal Development and Disorders 8
- Connexins and lens biology 3
- Hedgehog Signaling Pathway Studies 2
Cell Biology top 10%
Radiology, Nuclear Medicine and Imaging top 10%
- Retinal and Macular Surgery 4
Immunology
- interferon and immune responses 3

Co-authors: J. Fielding Hejtmancik Paul A. Sieving Rafael C. Caruso Habiba Chaâbouni Yong Zeng Ian M. MacDonald Yuri V. Sergeev Ridha Mrad
Cited by: Ophthalmology Genetics Molecular Biology
Journals: New England Journal of Medicine (1 paper)Human Molecular Genetics (2 papers)Investigative Ophthalmology & Visual Science (8 papers)
Partner nations: United States Tunisia France

In The Last Decade

Nizar Smaoui

28 papers receiving 921 citations

Peers

Countries citing papers authored by Nizar Smaoui

Since Specialization

Citations

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

Fields of papers citing papers by Nizar Smaoui

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Baseline TREM-1 Whole Blood Gene Expression Does Not Predict Response to Adalimumab Treatment in Patients with Ulcerative Colitis or Crohn’s Disease in the SERENE Studies Journal of Crohn s and Colitis ·Bram Verstockt,Valerie Pivorunas,Naim Al Mahi,Nizar Smaoui,Heath Guay,Nicholas A. Kennedy,James Goodhand,Simeng Lin,Benjamin Y H Bai,Stephen B. Hanauer,Marc Ferrante,Julián Panés,Séverine Vermeire	2023	3
2	De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy Annals of Clinical and Translational Neurology ·Sahar Esmaeeli Nieh,Maura R.Z. Madou,Minhajuddin Sirajuddin,Brieana Fregeau,Dianalee McKnight,Katrina W. Lexa,Jonathan B. Strober,Christine G. Spaeth,Barbara Hallinan,Nizar Smaoui,John Pappas,Thomas Andrew Burrow,Marie McDonald,Mariam Latibashvili,Esther Leshinsky‐Silver,Dorit Lev,Luba Blumkin,Ronald D. Vale,A. James Barkovich,Elliott H. Sherr	2015	76
3	Novel de novo SPOCK1 mutation in a proband with developmental delay, microcephaly and agenesis of corpus callosum European Journal of Medical Genetics ·Radhika Dhamija,John M. Graham,Nizar Smaoui,Erik C. Thorland,Salman Kirmani	2014	20
4	DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome Pediatric Nephrology ·Judy Savige,Elisabet Ars,Richard G.H. Cotton,David K. Crockett,Hayat Dagher,Constantinos Deltas,Jie Ding,Frances Flinter,Geneviève Pont-Kingdon,Nizar Smaoui,Roser Torrá,Helen Storey	2013	16
5	Exon-level array CGH in a large clinical cohort demonstrates increased sensitivity of diagnostic testing for Mendelian disorders Genetics in Medicine ·Swaroop Aradhya,Rachel Lewis,Tahrra Bonaga,Nnenna Nwokekeh,Amanda Stafford,Barbara A. Boggs,Kathleen S. Hruska,Nizar Smaoui,John G. Compton,Gabriele Richard,Sharon F. Suchy	2012	48
6	Molecular Analysis of Bardet-Biedl Syndrome Families: Report of 21 Novel Mutations in 10 Genes Investigative Ophthalmology & Visual Science ·Jianjun Chen,Nizar Smaoui,Monia Ben Hamed Hammer,Xiaodong Jiao,Sheikh Riazuddin,Shyana Harper,Nicholas Katsanis,Habiba Chaâbouni,Eliot L. Berson,J. Fielding Hejtmancik	2011	40
7	High-Throughput Retina-Array for Screening 93 Genes Involved in Inherited Retinal Dystrophy Investigative Ophthalmology & Visual Science ·Jin Won Song,Nizar Smaoui,Radha Ayyagari,David Stiles,Sonia Benhamed,Ian M. MacDonald,Stephen P. Daiger,Santa J. Tumminia,Fielding Hejtmancik,Xinjing Wang	2011	35
8	Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis Human Molecular Genetics ·Yuri V. Sergeev,Rafael C. Caruso,Meira R. Meltzer,Nizar Smaoui,Ian M. MacDonald,Paul A. Sieving	2010	53
9	The functional effect of pathogenic mutations in Rab escort protein 1 Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Yuri V. Sergeev,Nizar Smaoui,Ruifang Sui,David Stiles,N. Gordiyenko,N. Strunnikova,Ian M. MacDonald	2009	45
10	Null Retinoschisin-Protein Expression from anRS1c354del1-ins18 Mutation Causing Progressive and Severe XLRS in a Cross-Sectional Family Study Investigative Ophthalmology & Visual Science ·Camasamudram Vijayasarathy,Lucia Ziccardi,Yong Zeng,Nizar Smaoui,Rafael C. Caruso,Paul A. Sieving	2009	14
11	Structural Correlation Using Adaptive Optics Scanning Laser Ophthalmoscopy in X-Linked Retinoschisis Investigative Ophthalmology & Visual Science ·Jacque L. Duncan,Y. Zhang,S. Sundquist,Alexey V. Solovyev,Shuai Chang,Nizar Smaoui,Austin Roorda	2008	1
12	Choroideremia: Analysis of the Retina from a Female Symptomatic Carrier Ophthalmic Genetics ·Vera L. Bonilha,Karmen M Trzupek,Yong Li,Peter J. Francis,Joe G. Hollyfield,Mary E. Rayborn,Nizar Smaoui,Richard G. Weleber	2008	39
13	MEFV Mutations in Tunisian Patients Suffering from Familial Mediterranean Fever Seminars in Arthritis and Rheumatism ·Habiba Chaâbouni,Mohamed Ksantini,Ridha Mrad,Maher Kharrat,Myriam Châabouni,Faouzi Mâazoul,Zouhair Bahloul,Lamia Ben Jemâa,Fatma Ben Moussa,T. Ben Châabane,S. M’rad,Isabelle Touitou,Nizar Smaoui	2007	30
14	Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family Clinical Dysmorphology ·Myriam Châabouni,Nizar Smaoui,Neila Benneji,Ridha M rad,Lamia Ben Jemâa,Slah Hachicha,Habiba Chaâbouni	2004	14
15	Molecular Genetics of Cataract Developments in ophthalmology ·J. Fielding Hejtmancik,Nizar Smaoui	2003	59
16	Étude de l'association entre diabète type 1 et polymorphisme du gène CTLA-4 dans une population tunisienne Pathologie Biologie ·Haisam Abid,Slama Hmida,Nizar Smaoui,Houda Kâabi,Abdelmajid Abid,Habiba Chaâbouni,K. Boukef,K Nagati	2001	11
17	Prenatal diagnosis of chromosome disorders in Tunisian population#1Institute where the work was conducted is Service des Maladies Héréditaires et Congénitales Hôpital Charles Nicolle Tunis. Annales de Génétique ·H. Chaàbouni,Myriam Châabouni,Faouzi Mâazoul,Ridha Mrad,Lamia Ben Jemâa,Nizar Smaoui,Khaled Terras,H. Kammoun,Neila Belghith,Hana Ridene,B Oueslati,F. Zouari	2001	22
18	A Transcriptional Map of the FMF Region Genomics ·Alain Bernot,Roland Heilig,Christian Clépet,Nizar Smaoui,Corinne Da Silva,Jean‐Louis Petit,Catherine Devaud,Nuchanard Chiannilkulchai,Cécile Fizames,Delphine Samson,Corinne Cruaud,Christophe Caloustian,Gàbor Gyapay,Marc Delpech,Jean Weissenbach	1998	11
19	Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees. Journal of Medical Genetics ·Madeleine Dupont,Christiane Dross,Nizar Smaoui,Brigitte Nédelec,Gilles Grateau,Christian Clépet,I Gourdier,Isabelle Koné‐Paut,Marc Delpech,Jacques Demaille,Isabelle Touitou	1997	3
20	Structural Analysis of the Minisatellite Present at the 3' end of the Human Apolipoprotein B Gene: New Definition of the Alleles and Evolutionary Implications Human Molecular Genetics ·Catherine Burési,Érick Desmarais,Suzanne Vigneron,H. Lamarti,Nizar Smaoui,François Cambien,Gérard Roizès	1996	19

About Nizar Smaoui

Nizar Smaoui is a scholar working on Immunology and Allergy, Ophthalmology and Genetics, having authored 29 papers that have together received 938 indexed citations. Recurring topics across this work include Retinal Development and Disorders (8 papers), Retinal and Macular Surgery (4 papers), Genomics and Rare Diseases (3 papers), interferon and immune responses (3 papers), Connexins and lens biology (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). The work is most often cited by research in Ophthalmology (256 citations), Genetics (380 citations) and Molecular Biology (739 citations). Nizar Smaoui has collaborated with scholars based in United States, Tunisia and France. Frequent co-authors include J. Fielding Hejtmancik, Paul A. Sieving, Rafael C. Caruso, Habiba Chaâbouni, Yong Zeng, Ian M. MacDonald, Yuri V. Sergeev, Ridha Mrad, Faouzi Mâazoul and Ronald A. Bush. Their work appears in journals such as New England Journal of Medicine, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

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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