Neïla Belguith

495 citations

34 papers · 226 indexed · h-index 9

Co-authors: Faiza Fakhfakh Leila Keskes Hassen Kamoun Mouna Mnif M. Hachicha Emna Mkaouar‐Rebai Nadia Charfi Nozha Chakroun
Topics: RNA modifications and cancer (6 papers)Genetic and Kidney Cyst Diseases (6 papers)Sexual Differentiation and Disorders (5 papers)
Cited by: Endocrinology, Diabetes and Metabolism Genetics Reproductive Medicine
Journals: Biochemical and Biophysical Research Communications Gene Thyroid
Partner nations: Tunisia France Belgium

In The Last Decade

Neïla Belguith

33 papers receiving 221 citations

Peers

Countries citing papers authored by Neïla Belguith

Since Specialization

Citations

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

Fields of papers citing papers by Neïla Belguith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neïla Belguith

This figure shows the co-authorship network connecting the top 25 collaborators of Neïla Belguith. A scholar is included among the top collaborators of Neïla Belguith 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 Neïla Belguith. Neïla Belguith 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	Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation 2022 ·BMC Medical Genomics ·(unknown),(unknown),M. Chérif,(unknown),(unknown),(unknown),Neïla Belguith,Ridha Mrad	4
2	Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population 2022 ·The Journal of Steroid Biochemistry and Molecular Biology ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Leila Keskes,Mouna Mnif,Alex Odermatt,Neïla Belguith	2
3	Autosomal dominant polycystic kidney disease (ADPKD) in Tunisia: From molecular genetics to the development of prognostic tools 2022 ·Gene ·(unknown),Pascale Hilbert,Asma Ahmed,(unknown),(unknown),Hassen Kamoun,Leila Keskes,Neïla Belguith	1
4	Annexin A1 and its receptor gene polymorphisms in systemic lupus erythematosus in the Tunisian population 2022 ·Clinical Rheumatology ·(unknown),(unknown),Olfa Abida,(unknown),Nésrine Elloumi,Houda Kanoun,Neïla Belguith,S. Marzouk,R. Fakhfakh,(unknown),Héla Mnif,Hassen Kamoun,Z. Bahloul,Hatem Masmoudi	4
5	High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis 2021 ·Frontiers in Endocrinology ·Athanasia Stoupa,(unknown),(unknown),Dulanjalee Kariyawasam,Gabor Szinnai,Sylvain Hanein,Christine Bôle‐Feysot,Cécile Fourrage,Patrick Nitschké,Caroline Thalassinos,Graziella Pinto,Mouna Mnif,S. Baron,Marc de Kerdanet,Rachel Reynaud,Pascal Barat,M. Hachicha,Neïla Belguith,Michel Polak,Aurore Carré	17
6	First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy 2018 ·Biochemical and Biophysical Research Communications ·(unknown),(unknown),(unknown),Neïla Belguith,Leila Keskes,Emna Mkaouar‐Rebai,Faiza Fakhfakh	8
7	First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation 2018 ·Biochemical and Biophysical Research Communications ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Neïla Belguith,Leila Keskes,N. Gouider‐Khouja,Faiza Fakhfakh	2
8	Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene 2018 ·Gene ·(unknown),Pascale Hilbert,Asma Ahmed,(unknown),(unknown),(unknown),J. Hachicha,Hassen Kamoun,Leila Keskes,Neïla Belguith	4
9	Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect 2016 ·The Journal of Steroid Biochemistry and Molecular Biology ·(unknown),(unknown),Nadia Mahfoudh,(unknown),(unknown),Hassen Kamoun,Leila Keskes,Alex Odermatt,Neïla Belguith	11
10	First molecular diagnosis of Donohue syndrome in Africa: novel unusual insertion/deletion mutation in the INSR gene 2016 ·Molecular Biology Reports ·(unknown),(unknown),(unknown),(unknown),Neïla Belguith,Faiza Fakhfakh	3
11	Biochemical analyses and molecular modeling explain the functional loss of 17β-hydroxysteroid dehydrogenase 3 mutant G133R in three Tunisian patients with 46, XY Disorders of Sex Development 2015 ·The Journal of Steroid Biochemistry and Molecular Biology ·(unknown),(unknown),Christoph P. Sager,Maria Tsachaki,Julia Birk,Faiza Fakhfakh,Leila Keskes,Neïla Belguith,Alex Odermatt	14
12	Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect 2015 ·European Journal of Pediatrics ·(unknown),Nadia Charfi,Nabil Miled,(unknown),Neïla Belguith,Mouna Mnif,(unknown),(unknown),Hammadi Ayadi,M. Hachicha,M. Abid	3
13	First functional analysis of a novel splicing mutation in the B3GALTL gene by an ex vivo approach in Tunisian patients with typical Peters plus syndrome 2013 ·Gene ·(unknown),(unknown),Riadh Ben Mansour,(unknown),(unknown),Emna Mkaouar‐Rebai,Neïla Belguith,Faiza Fakhfakh	7
14	Novel double deletions in the MECP2 gene in Tunisian Rett patient 2012 ·Gene ·(unknown),(unknown),(unknown),Emna Mkaouar‐Rebai,Neïla Belguith,(unknown),Faiza Fakhfakh	3
15	Two Tunisian patients with Peters plus syndrome harbouring a novel splice site mutation in the B3GALTL gene that modulates the mRNA secondary structure 2012 ·Gene ·(unknown),Neïla Belguith,(unknown),(unknown),(unknown),I. Chabchoub,(unknown),Faiza Fakhfakh	8
16	Chromosomal defects in infertile men with poor semen quality 2012 ·Journal of Assisted Reproduction and Genetics ·(unknown),(unknown),Fatma Ben Abdallah,(unknown),(unknown),(unknown),Nozha Chakroun,Afifa Sellami,Neïla Belguith,Hassen Kamoun,(unknown),Leila Keskes	33
17	[Bardet - Biedl syndrome in the child. A study of 11 cases]. 2011 ·PubMed ·Hajer Aloulou,(unknown),Neïla Belguith,(unknown),(unknown),I. Chabchoub,(unknown),M. Hachicha	3
18	Descriptive analyses of Turner syndrome: 49 cases in Tunisia 2010 ·Annales d Endocrinologie ·(unknown),Moncef Feki,(unknown),Nadia Charfi,N. Rekik,(unknown),(unknown),Neïla Belguith,(unknown),Mohamed Tahar Sfar,M. Hachicha,M. Abid	10
19	Ganglioneuroma of adrenal gland in a patient with Turner syndrome 2009 ·Annals of Diagnostic Pathology ·Mahdi Kamoun,Mouna Mnif,N. Rekik,Neïla Belguith,Nadia Charfi,(unknown),(unknown),Fatma Mnif,(unknown),(unknown),Hassen Kamoun,Tahia Sellami‐Boudawara,M. Hachicha,M. Abid	12
20	Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases 2007 ·Biochemical and Biophysical Research Communications ·Emna Mkaouar‐Rebai,Abdelaziz Tlili,Saber Masmoudi,Neïla Belguith,Ilhem Charfeddine,Mouna Mnif,Chahnez Triki,Faiza Fakhfakh	19

About Neïla Belguith

Neïla Belguith is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Molecular Biology, having authored 34 papers that have together received 226 indexed citations. Recurring topics across this work include RNA modifications and cancer (6 papers), Genetic and Kidney Cyst Diseases (6 papers) and Sexual Differentiation and Disorders (5 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (76 citations), Genetics (123 citations) and Reproductive Medicine (30 citations). Neïla Belguith has collaborated with scholars based in Tunisia, France and Belgium. Frequent co-authors include Faiza Fakhfakh, Leila Keskes, Hassen Kamoun, Mouna Mnif, M. Hachicha, Emna Mkaouar‐Rebai, Nadia Charfi, Nozha Chakroun, Chahnez Triki and Afifa Sellami. Their work appears in journals such as Biochemical and Biophysical Research Communications, Gene and Thyroid.

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