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Abdelhamid Barakat

genomics and human genetics laboratory

29H指数
195论文数
2.6K被引数
收录论文 47
发表时间
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Mutational spectrum of SLC26A4 and SLC26A5 associated with hereditary hearing loss in Moroccan families与摩洛哥家庭遗传性耳聋相关的SLC26A4和SLC26A5突变谱
errHuman Genomics
IF4.3
err2026-07-01
err0
errOAAI
errAssia Idyahia; Salaheddine Redouane; Fatima Ezzahra Chentoufi; Hicham Charoute; Adil El Hamouchi; Houda Benrahma; Abdelhamid Barakat
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Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2通过外显子测序扩展摩洛哥家庭的神经遗传疾病遗传谱：在RYR3、POLR3A和LAMA2中鉴定候选变异
errMolecular Biology Reports
IF2.8
err2026-05-11
err0
PREAI
errFatima Ezzahra Chentoufi; Assia Idyahia; Madoussou Toure; Adil El Hamouchi; Abdelhamid Barakat; Houda Benrahma; Hicham Charoute
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err收藏
Identification of deleterious missense variants of serine peptidase inhibitor Kazal type 2 gene and their impact on KAZAL domain structure, stability, flexibility, and dimension
errJournal of Biomolecular Structure and Dynamics
IF2.4
err2026-01-30
err0
PREAI
errGhita Elkarhat; Samah Ait Benichou; Salaheddine Redouane; Abdelhamid Barakat; Abdelaziz Soukri; Bouchra El Khalfi; Hassan Rouba
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Impact of TNF-α (− 308G>A and − 857 C>T) promoter variants on susceptibility to chronic hepatitis B virus infection in a cohort of Mauritanian patients: pilot study
errBMC Microbiology
IF4.2
err2026-01-15
err0
errOAAI
errSaffiya Mounira Ennahoui; Abdallah Sid M’Hamed; Fatimetou Veten; Sidi M. Cheikh Bouna; Abdelhamid Barakat; Tetou Soumbara; Ahmed Houmeida
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Disorders of sex development associated with MPI and RSPH1 variants expand the phenotypic spectrum of CDG and PCD in Morocco
errMolecular Biology Reports
IF2.8
err2026-01-14
err0
PREAI
errHouda Harmak; Salaheddine Redouane; Adil El Hamouchi; Hicham Charoute; Ouafaa Aniq Filali; Rachid Aboutaieb; Abdelhamid Barakat; Hassan Rouba
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Emergence of rare SARS-CoV-2 subvariant LF.7.3 obtained from Moroccan COVID-19 patients来自摩洛哥COVID-19患者的罕见SARS-CoV-2亚变种LF.7.3的出现
errMicrobiology Resource Announcements
IF0.6
err2026-01-01
err0
PREAI
errGhammaz, Hamza; El Hamouchi, Adil; Touil, Nadia; El Annaz, Hicham; Melloul, Marouane; Barakat, Abdelhamid; El Fahime, Elmostafa
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Understanding the molecular basis of radioresistance in lung cancer: A comprehensive review理解肺癌放射抵抗的分子基础：一项综合综述
errEurasian Journal of Medicine and Oncology
IF0.7
err2026-01-01
err0
PREAI
errAttouahri, Fatima Zohra; Addoum, Boutaina; Benbacer, Leila; Mimount, Samira; El Mchichi, Bouchra; Barakat, Abdelhamid; El Ouazzani, Hanane; Rhorfi, Ismail; Abid, Ahmed; Ababou, Mouna; Ennibi, Khalid; Errafii, Khaoula; El Mzibri, Mohammed
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In silico analysis of missense SNPs in APPL1 gene: implications on APPL1-AKT2 complex and its relation to MODY 14APPL1基因错义SNP的计算机模拟分析：对APPL1-AKT2复合物及其与MODY 14关系的启示
errJOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
IF2.4
err2025-11-01
err0
PREAI
errSlaoui, Kenza; Hami, Hinde; Redouane, Salaheddine; Charoute, Hicham; El Khair, Kenza; Soulaymani, Abdelmajid; Barakat, Abdelhamid
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Computational study of deleterious missense SNPs in the USH1G gene implicated in Usher syndrome计算研究与Usher综合征相关的USH1G基因中有害错义SNPs
errJournal of Biomolecular Structure and Dynamics
IF2.4
err2025-09-02
err0
PREAI
errKenza El Khair; Madoussou Toure; Salaheddine Redouane; Hicham Charoute; Kenza Slaoui; Houda Benrahma; Abdelhamid Barakat
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Novel splice variants implicated in inherited retinal dystrophies in two Moroccan families在两个摩洛哥家庭中与遗传性视网膜变性疾病相关的 Novel splice variants
errMolecular Biology Reports
IF2.8
err2025-08-12
err0
PREAI
errKenza El Khair; Aymane Bouzidi; Majida Charif; Hicham Charoute; Adil El Hamouchi; Hanane Serraj Filali; Houda Benrahma; Guy Lenaers; Abdelhamid Barakat
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Computational study of the potential impact of WHRN protein missense SNPs on WHRN-MYO15A protein complex interaction and their association with Usher syndromeWHRN蛋白错义SNP对WHRN-MYO15A蛋白复合物相互作用及其与Usher综合征关联的潜在影响的计算研究
errJOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
IF2.4
err2025-05-19
err0
PREAI
errFatima Ezzahra Chentoufi; Salaheddine Redouane; Abdelhamid Barakat; Houda Benrahma; Hicham Charoute
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Missense variants weakening a SOX9 phosphodegron linked to odontogenesis defects, scoliosis, and other skeletal features
errHUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
err2025-04-01
err0
errOAAI
errEttaki, Imane; Haseeb, Abdul; Karvande, Anirudha; Amalou, Ghita; Saih, Asmae; Aitraise, Imane; Hamdi, Salsabil; Wakrim, Lahcen; Barakat, Abdelhamid; Fellah, Hassan; El Alloussi, Mustapha; Lefebvre, Veronique
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Establishing African genomics and bioinformatics programs through annual regional workshops
errNATURE GENETICS
IF31.8
err2024-07-08
err0
PREAI
errSharaf, Abdoallah; Nesengani, Lucky Tendani; Hayah, Ichrak; Kuja, Josiah Ochieng; Mdyogolo, Sinebongo; Omotoriogun, Taiwo Crossby; Odogwu, Blessing Adanta; Beedessee, Girish; Smith, Rae Marvin; Barakat, Abdelhamid; Moila, Acclaim M.; El Hamouchi, Adil; Benkahla, Alia; Boukteb, Amal; Elmouhtadi, Amine; Mafwila, Antoine Lusala; Abushady, Asmaa Mohammed; Elsherif, Assem Kadry; Ahmed, Bulbul; Wairuri, Charles; Ndiribe, Charlotte C.; Ebuzome, Chukwuike; Kinnear, Craig J.; Ndlovu, Deborah-Fay; Iraqi, Driss; El Fahime, Elmostafa; Assefa, Ermias; Ouardi, Faissal; Belharfi, Fatima Zohra; Tmimi, Fatim Zohra; Markey, Fatu Badiane; Radouani, Fouzia; Zeukeng, Francis; Mvumbi, Georges Lelo; Ganesan, Hamilton; Hanachi, Mariem; Nigussie, Helen; Charoute, Hicham; Benamri, Ichrak; Mkedder, Ikram; Haddadi, Imane; Meftah-Kadmiri, Issam; Mubiru, Jackson Franco; Domelevo Entfellner, Jean-Baka Kodjo; Rokani, Joan Bayowa; Ogwang, Joel; Daiga, Jude Bigoga; Omumbo, Judy; Ideozu, Justin Eze; Errafii, Khaoula; Labuschagne, Kim; Komi, Komi Koukoura; Tonfack, Libert Brice; Hadjeras, Lydia; Ramantswana, Madeleine; Chaisi, Mamohale; Botes, Marietjie W.; Kilian, Mariette; Kvas, Marija; Melloul, Marouane; Chaouch, Melek; Khyatti, Meriem; Abdo, Michael; Phasha-Muchemenye, Mmatshepho; Hijri, Mohamed; Mediouni, Mohammed Rida; Hassan, Mohammed Ahmed; Piro, Mohammed; Mwale, Monica; Maaloum, Mossaab; Mavhunga, Mudzuli; Olivier, Nicholas Abraham; Aminou, Oumaima; Arbani, Oumayma; Souiai, Oussema; Djocgoue, Pierre Francois; Mentag, Rachid; Zipfel, Renate Dorothea; Tata, Rolland Bantar; Megnekou, Rosette; Muzemil, Sadik; Paez, Sadye; Salifu, Samson Pandam; Kagame, Samuel Paul; Selka, Sarra; Edwards, Sean; Gaouar, Semir Bechir Suheil; Reda, Shaimaa Roshdy Abdullah; Fellahi, Siham; Khayi, Slimane; Ayed, Soumia; Madisha, Thabang; Sahil, Tulsi; Udensi, Ogbuagu Ugorji; Ras, Verena; Ezebuiro, Victor; Duru, Vincent C.; David, Xavier; Geberemichael, Yonas; Tchiechoua, Yves H.; Mungloo-Dilmohamud, Zahra; Chen, Zhiliang; Happi, Christian; Kariuki, Thomas; Ziyomo, Cathrine; Djikeng, Appolinaire; Badaoui, Bouabid; Mapholi, Ntanganedzeni; Muigai, Anne; Osuji, Julian O.; Ebenezer, ThankGod Echezona
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Optimizing diagnosis of neuromuscular diseases by high-through-put sequencing: Genetic characterization and classification of sequence variants
errCLINICA CHIMICA ACTA
IF2.9
err2024-05-01
err0
PREAI
errRochdi, K.; Cerino, M.; Da Silva, N.; Delague, V.; Nahili, H.; Kriouile, Y.; Gorokhova, S.; Bartoli, M.; Saile, R.; Barakat, A.; Krahn, M.
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Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2022-05-12
err10
errOAAI
errBouzidi, Aymane; Charoute, Hicham; Charif, Majida; Amalou, Ghita; Kandil, Mostafa; Barakat, Abdelhamid; Lenaers, Guy
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err收藏
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysisHNF1A基因变异和单倍型与代谢综合征的关联: 突尼斯人群的病例对照研究和荟萃分析
errDIABETOLOGY & METABOLIC SYNDROME
IF3.9
err2022-02-02
err5
errOAAI
errDallali, Hamza; Hechmi, Meriem; Morjane, Imane; Elouej, Sahar; Jmel, Haifa; Ben Halima, Yosra; Abid, Abdelmajid; Bahlous, Afef; Barakat, Abdelhamid; Jamoussi, Henda; Abdelhak, Sonia; Kefi, Rym
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Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder
errCLINICA CHIMICA ACTA
IF2.9
err2022-01-01
err5
errOAAI
errRochdi, Khaoula; Cerino, Mathieu; Da Silva, Nathalie; Delague, Valerie; Bouzidi, Aymane; Nahili, Halima; Zouiri, Ghizlane; Kriouile, Yamna; Gorokhova, Svetlana; Bartoli, Marc; Saile, Rachid; Barakat, Abdelhamid; Krahn, Martin
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err收藏
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy
errBRAIN COMMUNICATIONS
IF4.5
err2021-04-07
err25
errOAAI
errCharif, Majida; Gueguen, Naig; Ferre, Marc; Elkarhat, Zouhair; Khiati, Salim; LeMao, Morgane; Chevrollier, Arnaud; Desquiret-Dumas, Valerie; Goudenege, David; Bris, Celine; Kane, Selma; Alban, Jennifer; Chupin, Stephanie; Wetterwald, Celine; Caporali, Leonardo; Tagliavini, Francesca; LaMorgia, Chiara; Carbonelli, Michele; Jurkute, Neringa; Barakat, Abdelhamid; Gohier, Philippe; Verny, Christophe; Barth, Magalie; Procaccio, Vincent; Bonneau, Dominique; Zanlonghi, Xavier; Meunier, Isabelle; Weisschuh, Nicole; Schimpf-Linzenbold, Simone; Tonagel, Felix; Kellner, Ulrich; Yu-Wai-Man, Patrick; Carelli, Valerio; Wissinger, Bernd; Amati-Bonneau, Patrizia; Reynier, Pascal; Lenaers, Guy
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Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africars662799变异和APOA5基因单倍型与代谢综合征及其组分的关联: 北非的meta分析
errBIOSCIENCE REPORTS
IF4.7
err2020-08-13
err11
errOAAI
errHechmi, Meriem; Dallali, Hamza; Gharbi, Meriem; Jmel, Haifa; Fassatoui, Meriem; Ben Halima, Yossra; Bahri, Sonia; Bahlous, Afaf; Abid, Abdelmajid; Jamoussi, Henda; Barakat, Abdelhamid; Kefi, Rym
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Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families
errJOURNAL OF CLINICAL IMMUNOLOGY
IF5.7
err2019-11-06
err8
PREAI
errBen-Ali, Meriem; Kechout, Nadia; Mekki, Najla; Yang, Jing; Chan, Koon Wing; Barakat, Abdelhamid; Aadam, Zahra; Gamara, Jouda; Gargouri, Lamia; Largueche, Beya; BelHadj-Hmida, Nabil; Nedri, Amel; Ben Ameur, Houcine; Mellouli, Fethi; Boukari, Rachida; Bejaoui, Mohamed; Bousfiha, Aziz; Ben-Mustapha, Imen; Lau, Yu-Lung; Barbouche, Mohamed-Ridha
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研究方向

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合作学者
合作期刊
P
Patrick F. Chinnery
H 指数: 128 · 论文数: 939
P
Peter Nürnberg
H 指数: 127 · 论文数: 756
K
Kay Hofmann
H 指数: 111 · 论文数: 473
J
Joris A. Veltman
H 指数: 102 · 论文数: 405
V
Valério Carelli
H 指数: 94 · 论文数: 733
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