Hassen Kamoun - Publications, H-index & Citations

Hassen Kamoun

hedi chaker hospital

17H指数

113论文数

719被引数

收录论文 19

发表时间

Comprehensive Genomic Profiling Reveals the Mutational Spectrum and Clinical Significance of BRCA1/2 and Other Cancer-Susceptibility Genes in Breast Cancer Patients from Southern Tunisia 综合基因组分析揭示了突变的谱系和临床意义，以及突变的BRCA1/2和其他癌症易感基因在突尼斯南部乳腺癌患者中的临床意义

Cancers

IF4.4

2026-08-29

OAAI

Nihel Ammous-Boukhris; Rania Abdelmaksoud-Dammak; Wala Ben Kridis; Dorra Ben-Ayed-Guerfali; Souhir Guidara; Ameni Feki; Hassen Kamoun; Afef Khanfir; Jamel Daoud; Gérard-Hubert Lizard; Ali Gargouri; Raja Mokdad-Gargouri

Genetic investigation of a Tunisian family with Lynch syndrome: a case report

Frontiers in Oncology

IF3.3

2026-01-20

OAAI

Rania Abdelmaksoud-Dammak; Nihel Ammous-Boukhris; Souhir Guidara; Slim Charfi; Ameni Feki; Manel Guirat; Rahma Daoud; Hassen Kamoun; Tahya Sellami-Boudawara; Afef Khanfir; Raja Mokdad-Gargouri

Germline and somatic mutational variants of Tunisian high grade serous ovarian cancer identified by next-generation sequencing 通过下一代测序鉴定出的突尼斯高级别浆液性卵巢癌的生殖系和体细胞突变变体

BMC Cancer

IF3.4

2025-10-11

OAAI

Nihel Ammous-Boukhris; Rania Abdelmaksoud-Dammak; Wala Ben Kridis; Dorra Ben-Ayed-Guerfali; Arwa Shtaiwi Abed; Souhir Guidara; Slim Charfi; Ameni Feki; Tahia Sellami-Boudawara; Hassen Kamoun; Afef Khanfir; Jamel Daoud; Raja Mokdad-Gargouri

Psychological impact of motor impairment in tow forms of congenital muscular dystrophy

EUROPEAN PSYCHIATRY

IF6.7

2023-07-19

OAAI

Boujelbene, I.; Chaabane, M.; Guirat, M.; Ben Touhemi, D.; Gharbi, N.; Yousr, M.; Kamoun, H.; Ben Ayed, I.

Familial Autism Spectrum Disorder : A clinical study from South Tunisia

EUROPEAN PSYCHIATRY

IF6.7

2023-07-19

OAAI

Boujelben, I.; Chaabane, M.; Ben Ayed, I.; Ben Touhemi, D.; Gharbi, N.; Guirat, M.; HajKacem, I.; Ayadi, H.; Kamoun, H.; Moalla, Y.

The psychological impact on parents of children with pyridoxine-dependent epilepsy

EUROPEAN PSYCHIATRY

IF6.7

2023-07-19

OAAI

Boujelbene, I.; Chaabane, M.; Guirat, M.; Ben Touhemi, D.; Guidara, S.; Moalla, Y.; Kamoun, H.; Ben Ayed, I.

Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population

JOURNAL OF ADVANCED RESEARCH

IF13

2021-07-01

OAAI

Souissi, Amal; Ben Said, Mariem; Ben Ayed, Ikhlas; Elloumi, Ines; Bouzid, Amal; Mosrati, Mohamed Ali; Hasnaoui, Mehdi; Belcadhi, Malek; Idriss, Nabil; Kamoun, Hassen; Gharbi, Nourhene; Gibriel, Abdullah A.; Tlili, Abdelaziz; Masmoudi, Saber

Detection of a novel mutation in a Tunisian child with polycystic kidney disease

IUBMB LIFE

IF3.2

2020-05-30

OAAI

Abdelwahed, Mayssa; Hilbert, Pascale; Ahmed, Asma; Dey, Mouna; Kamoun, Hassen; Ammar-Keskes, Leila; Belguith, Neila

A novel disease-causing mutation in the Renin gene in a Tunisian family with autosomal dominant tubulointerstitial kidney disease

INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

IF2.8

2019-12-01

PREAI

Abdelwahed, Mayssa; Chaabouni, Yosr; Michel-Calemard, Laurence; Chaabouni, Khansa; Morel, Yves; Hachicha, Jamil; Makni, Fatma Ayedi; Kamoun, Hassen; Ammar-Keskes, Leila; Belghith, Neila

A homozygous ABCB4 mutation causing an LPAC syndrome evolves into cholangiocarcinoma

CLINICA CHIMICA ACTA

IF2.9

2019-08-01

PREAI

Khabou, Boudour; Trigui, Ayman; Boudawara, Tahya Sellami; Keskes, Leila; Kamoun, Hassen; Barbu, Veronique; Fakhfakh, Faiza

A novel de novo splicing mutation c.1444-2A>T in the TSC2 gene causes exon skipping and premature termination in a patient with tuberous sclerosis syndrome

IUBMB LIFE

IF3.2

2019-07-18

OAAI

Abdelwahed, Mayssa; Touraine, Renaud; Ben-Rhouma, Bochra; Dhieb, Dhoha; Mars, Manel; Kammoun, Khawla; Hachicha, Jamil; Triki, Chahnez; Kamoun, Hassen; Keskes-Ammar, Leila; Belguith, Neila

Altered three-dimensional organization of sperm genome in DPY19L2-deficient globozoospermic patients

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2018-10-25

OAAI

Abdelhedi, Fatma; Chalas, Celine; Petit, Jean-Maurice; Abid, Nouha; Mokadem, Elyes; Hizem, Syrine; Kamoun, Hassen; Keskes, Leila; Dupont, Jean-Michel

Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation 由p.Gln316Pro新突变引起的突尼斯X连锁肾上腺脑白质营养不良家庭的表型变异

CLINICA CHIMICA ACTA

IF2.9

2016-01-01

PREAI

Kallabi, Fakhri; Ellouz, Emna; Tabebi, Mouna; Ben Salah, Ghada; Kaabechi, Naziha; Keskes, Leila; Triki, Chahnez; Kamoun, Hassen

Chromosomal instability associated with a novel BLM frameshift mutation (c.1980-1982delAA) in two unrelated Tunisian families with Bloom syndrome

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

IF8

2013-10-01

PREAI

Ben Salah, G.; Salem, I. Hadj; Masmoudi, A.; Ben Rhouma, B.; Turki, H.; Fakhfakh, F.; Ayadi, H.; Kamoun, H.

A Novel Nonsense Mutation in HSD17B3 Gene in a Tunisian Patient with Sexual Ambiguity

JOURNAL OF SEXUAL MEDICINE

IF3.3

2013-10-01

PREAI

Ben Rhouma, Bochra; Belguith, Neila; Mnif, Mouna Feki; Kamoun, Thouraya; Charfi, Nadia; Kamoun, Mahdi; Abdelhedi, Fatma; Hachicha, Mongia; Kamoun, Hassen; Abid, Mohamed; Fakhfakh, Faiza

Chromosomal Aberrations (CA), Sister Chromatid Exchanges (SCE), and High-Frequency Cells (HFC) Frequencies in Peripheral Blood Lymphocytes of Tunisian Gasoline Truck Loaders

HUMAN AND ECOLOGICAL RISK ASSESSMENT

IF2.7

2012-07-09

PREAI

Ben Salah, Ghada; Kamoun, Hassen; Rebai, Ahmed; Hajji, Rafika; Masmoudi, Mohamed-Elaarbi; Ayadi, Hamadi; Fakhfakh, Faiza

Chromosomal defects in infertile men with poor semen quality

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2012-03-11

OAAI

Ghorbel, Myriam; Baklouti, Siwar Gargouri; Ben Abdallah, Fatma; Zribi, Nacira; Cherif, Mariem; Keskes, Rim; Chakroun, Nozha; Sellami, Afifa; Belguith, Neila; Kamoun, Hassen; Fakhfakh, Faiza; Ammar-Keskes, Leila

Hematotoxicity and Genotoxicity of Mercuric Chloride Following Subchronic Exposure Through Drinking Water in Male Rats

BIOLOGICAL TRACE ELEMENT RESEARCH

IF3.6

2012-02-15

PREAI

Boujbiha, Mohamed Ali; Ben Salah, Ghada; Ben Feleh, Abdelraouf; Saoudi, Mongi; Kamoun, Hassen; Bousslema, Ali; Ommezzine, Asma; Said, Khaled; Fakhfakh, Faiza; El Feki, Abdelfattah

Effect of ENPP1/PC-1-K121Q and PPARγ-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population

DIABETES RESEARCH AND CLINICAL PRACTICE

IF7.4

2008-09-01

PREAI

Bouhaha, R.; Meyre, D.; Kamoun, H. Abid; Ennafaa, H.; Vaillant, E.; Sassi, R.; Baroudi, T.; Vatin, V.; Froguel, P.; Elgaaied, A.; Vaxillaire, M.

研究方向