Works matching AU Rouba, Hassan

Results: 35

Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 3, p. 499, doi. 10.1007/s10815-018-1373-4

By:

Elkarhat, Zouhair;
Kindil, Zineb;
Zarouf, Latifa;
Razoki, Lunda;
Aboulfaraj, Jamila;
Elbakay, Chadli;
Nassereddine, Sanaa;
Nasser, Boubker;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Whole exome sequencing reveals ABCD1 variant as a potential contributor to male infertility.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10234-7

By:

Redouane, Salaheddine;
Harmak, Houda;
El Hamouchi, Adil;
Charoute, Hicham;
Louanjli, Noureddine;
Malki, Abderrahim;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.

Published in:

Human Mutation, 2015, v. 36, n. 11, p. E2441, doi. 10.1002/humu.22835

By:

Charoute, Hicham;
Bakhchane, Amina;
Benrahma, Houda;
Romdhane, Lilia;
Gabi, Khalid;
Rouba, Hassan;
Fakiri, Malika;
Abdelhak, Sonia;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.

Published in:

Journal of Diabetes Research, 2019, p. 1, doi. 10.1155/2019/4951627

By:

Elkhattabi, Lamiae;
Morjane, Imane;
Charoute, Hicham;
Amghar, Soumaya;
Bouafi, Hind;
Elkarhat, Zouhair;
Saile, Rachid;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

Article

Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034902

By:

Eloualid, Abdelmajid;
Rhaissi, Houria;
Reguig, Ahmed;
Bounaceur, Safaa;
houate, Brahim El;
Abidi, Omar;
Charif, Majida;
Louanjli, Noureddine;
Chadli, Elbakkay;
Barakat, Abdelhamid;
Bashamboo, Anu;
McElreavey, Ken;
Rouba, Hassan

Publication type:

Article

Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility.

Published in:

PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0034111

By:

Eloualid, Abdelmajid;
Abidi, Omar;
Charif, Majida;
houate, Brahim El;
Benrahma, Houda;
Louanjli, Noureddine;
Chadli, Elbakkay;
Ajjemami, Maria;
Barakat, Abdelhamid;
Bashamboo, Anu;
McElreavey, Ken;
Rhaissi, Houria;
Rouba, Hassan

Publication type:

Article

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population.

Published in:

Mitochondrial DNA. Part A, 2018, v. 29, n. 1, p. 9, doi. 10.1080/24701394.2016.1233530

By:

Charoute, Hicham;
Kefi, Rym;
Bounaceur, Safaa;
Benrahma, Houda;
Reguig, Ahmed;
Kandil, Mostafa;
Rouba, Hassan;
Bakhchane, Amina;
Abdelhak, Sonia;
Barakat, Abdelhamid

Publication type:

Article

Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1516, doi. 10.1002/ajmg.a.61257

By:

Elkarhat, Zouhair;
Belkady, Boutaina;
Charoute, Hicham;
Zarouf, Latifa;
Razoki, Lunda;
Aboulfaraj, Jamila;
Nassereddine, Sanaa;
Elbakay, Chadli;
Nasser, Boubker;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Sex chromosome mosaicism in males carrying Y chromosome long arm deletions.

Published in:

2000

By:

Siffroi, Jean Pierre;
Le Bourhis, Corine;
Krausz, Csilla;
Barbaux, Sandrine;
Quintana-Murci, Luis;
Kanafani, Samia;
Rouba, Hassan;
Bujan, Louis;
Bourrouillou, Georges;
Seifer, Isabelle;
Boucher, Daniel;
Fellous, Marc;
McElreavey, Ken;
Dadoune, Jean Pierre;
Siffroi, J P;
Le Bourhis, C;
Krausz, C;
Barbaux, S;
Quintana-Murci, L;
Kanafani, S

Publication type:

journal article

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.

Published in:

PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0176516

By:

Bakhchane, Amina;
Charif, Majida;
Bousfiha, Amale;
Boulouiz, Redouane;
Nahili, Halima;
Rouba, Hassan;
Charoute, Hicham;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

Phylogeography of E1b1b1b-M81 Haplogroup and Analysis of Its Subclades in Morocco.

Published in:

Human Biology, 2014, v. 86, n. 2, p. 105, doi. 10.3378/027.086.0204

By:

Reguig, Ahmed;
Harich, Nourdin;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Y-Chromosome Analysis in Egypt Suggests a Genetic Regional Continuity in Northeastern Africa.

Published in:

Human Biology, 2002, v. 74, n. 5, p. 645, doi. 10.1353/hub.2002.0054

By:

Manni, Franz;
Leonardi, Pascal;
Barakat, Abdelhamid;
Rouba, Hassan;
Heyer, Evelyne;
Klintschar, Michael;
Mcelreavey, Ken;
Quintana-Murci, Lluís

Publication type:

Article

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the<bold><italic> R-spondin1 </italic></bold>Gene Associated with Familial 46,XX DSD.

Published in:

Sexual Development, 2017, v. 11, n. 5/6, p. 269, doi. 10.1159/000485393

By:

Naasse, Yassine;
Bakhchane, Amina;
Charoute, Hicham;
Jennane, Farida;
Bignon-Topalovic, Joelle;
Malki, Abderrahim;
Bashamboo, Anu;
Barakat, Abdelhamid;
Rouba, Hassan;
McElreavey, Ken

Publication type:

Article

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 3, p. 322, doi. 10.1038/ejhg.2013.151

By:

Charoute, Hicham;
Nahili, Halima;
Abidi, Omar;
Gabi, Khalid;
Rouba, Hassan;
Fakiri, Malika;
Barakat, Abdelhamid

Publication type:

Article

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco.

Published in:

2015

By:

Naasse, Yassine;
Charoute, Hicham;
El Houate, Brahim;
Elbekkay, Chadli;
Razoki, Lunda;
Malki, Abderrahim;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

journal article

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study.

Published in:

BioMed Research International, 2020, p. 1, doi. 10.1155/2020/7614634

By:

Ait El Cadi, Chaimaa;
Krami, Al Mehdi;
Charoute, Hicham;
Elkarhat, Zouhair;
Sifeddine, Najat;
Lakhiari, Hamid;
Rouba, Hassan;
Barakat, Abdelhamid;
Nahili, Halima

Publication type:

Article

Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/4872101

By:

Al Mehdi, Krami;
Fouad, Benhnini;
Zouhair, Elkarhat;
Boutaina, Belkady;
Yassine, Naasse;
Chaimaa, Ait El Cadi;
Najat, Sifeddine;
Hassan, Rouba;
Rachida, Roky;
Abdelhamid, Barakat;
Halima, Nahili

Publication type:

Article

Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/1832084

By:

Bouafi, Hind;
Bencheikh, Sara;
Mehdi Krami, A. L.;
Morjane, Imane;
Charoute, Hicham;
Rouba, Hassan;
Saile, Rachid;
Benhnini, Fouad;
Barakat, Abdelhamid

Publication type:

Article

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.

Published in:

Molecular Biology Reports, 2022, v. 49, n. 5, p. 3949, doi. 10.1007/s11033-022-07245-z

By:

AitRaise, Imane;
Amalou, Ghita;
Bousfiha, Amale;
Charoute, Hicham;
Rouba, Hassan;
Abdelghaffar, Houria;
Bonnet, Crystel;
Petit, Christine;
Barakat, Adbelhamid

Publication type:

Article

Novel compound heterozygous mutations in the GPR98 ( USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Published in:

Molecular Biology Reports, 2017, v. 44, n. 5, p. 429, doi. 10.1007/s11033-017-4129-9

By:

Bousfiha, Amale;
Bakhchane, Amina;
Charoute, Hicham;
Detsouli, Mustapha;
Rouba, Hassan;
Charif, Majida;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

TNF A −308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.

Published in:

Molecular Biology Reports, 2014, v. 41, n. 9, p. 5805, doi. 10.1007/s11033-014-3454-5

By:

Sefri, Hajar;
Benrahma, Houda;
Charoute, Hicham;
Lakbakbi el yaagoubi, Fouzia;
Rouba, Hassan;
Lyoussi, Badiaa;
Nourlil, Jalal;
Abidi, Omar;
Barakat, Abdelhamid

Publication type:

Article

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.

Published in:

Molecular Biology Reports, 2012, v. 39, n. 12, p. 11011, doi. 10.1007/s11033-012-2003-3

By:

Charif, Majida;
Bounaceur, Safaa;
Abidi, Omar;
Nahili, Halima;
Rouba, Hassan;
Kandil, Mostafa;
Boulouiz, Redouane;
Barakat, Abdelhamid

Publication type:

Article

Computational Analysis of nsSNPs of Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.

Published in:

2019

By:

Essadssi, Soukaina;
Krami, Al Mehdi;
Elkhattabi, Lamiae;
Elkarhat, Zouhair;
Amalou, Ghita;
Abdelghaffar, Houria;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

journal article

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

Published in:

Lipids in Health & Disease, 2014, v. 13, n. 1, p. 60, doi. 10.1186/1476-511X-13-60

By:

Ouatou, Sanaa;
Ajjemami, Maria;
Charoute, Hicham;
Sefri, Hajar;
Ghalim, Noreddine;
Rhaissi, Houria;
Benrahma, Houda;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

Published in:

Asian Journal of Andrology, 2007, v. 9, n. 5, p. 674, doi. 10.1111/j.1745-7262.2007.00290.x

By:

Imken, Laila;
El Houate, Brahim;
Chafik, Abdelaziz;
Nahili, Halima;
Boulouiz, Redouane;
Abidi, Omar;
Chadli, Elbakkay;
Louanjli, Noureddine;
Elfath, Abdelouhab;
Hassar, Mohammed;
McElreavey, Ken;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.

Published in:

Human Heredity, 2018, v. 83, n. 5, p. 274, doi. 10.1159/000499710

By:

Belkady, Boutaina;
Elkhattabi, Lamiae;
Elkarhat, Zouhair;
Zarouf, Latifa;
Razoki, Lunda;
Aboulfaraj, Jamila;
Nassereddine, Sanaa;
Cadi, Rachida;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

Article

Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population.

Published in:

Journal of Community Health, 2011, v. 36, n. 6, p. 943, doi. 10.1007/s10900-011-9393-3

By:

Benrahma, Houda;
Arfa, Imen;
Charif, Majida;
Bounaceur, Safaa;
Eloualid, Abdelmajid;
Boulouiz, Redouane;
Nahili, Halima;
Abidi, Omar;
Rouba, Hassan;
Chadli, Asmaa;
Oudghiri, Mounia;
Farouqui, Ahmed;
Abdelhak, Sonia;
Barakat, Abdelhamid

Publication type:

Article

Dialogical factors in toddlers’ use of clitic pronouns.

Published in:

First Language, 2010, v. 30, n. 3/4, p. 375, doi. 10.1177/0142723710379957

By:

Salazar Orvig, Anne;
Marcos, Haydée;
Morgenstern, Aliyah;
Hassan, Rouba;
Leber-Marin, Jocelyne;
Parès, Jacques

Publication type:

Article

Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case-Control Study and Meta-analysis.

Published in:

Biochemical Genetics, 2014, v. 52, n. 9/10, p. 430, doi. 10.1007/s10528-014-9658-5

By:

Benrahma, Houda;
Charoute, Hicham;
Lasram, Khaled;
Boulouiz, Redouane;
Atig, Rym;
Fakiri, Malika;
Rouba, Hassan;
Abdelhak, Sonia;
Barakat, Abdelhamid

Publication type:

Article

Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses.

Published in:

Journal of Biomolecular Structure & Dynamics, 2022, v. 40, n. 1, p. 361, doi. 10.1080/07391102.2020.1813628

By:

Elkarhat, Zouhair;
Charoute, Hicham;
Elkhattabi, Lamiae;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Identification of deleterious missense variants of human Piwi like RNA-mediated gene silencing 1 gene and their impact on PAZ domain structure, stability, flexibility and dimension: in silico analysis.

Published in:

2020

By:

Elkarhat, Zouhair;
Elkhattabi, Lamiaa;
Charoute, Hicham;
Morjane, Imane;
Errouagui, Abdellatif;
Carey, Francis;
Nasser, Boubker;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Letter

Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility.

Published in:

BioMed Research International, 2022, p. 1, doi. 10.1155/2022/1664825

By:

Harmak, Houda;
Charoute, Hicham;
Redouane, Salaheddine;
Filali, Ouafaa Aniq;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis.

Published in:

Cardiology Research & Practice, 2020, p. 1, doi. 10.1155/2020/5981971

By:

Morjane, Imane;
Charoute, Hicham;
Ouatou, Sanaa;
Elkhattabi, Lamiae;
Benrahma, Houda;
Saile, Rachid;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

Article

In silico exploration and molecular dynamics of deleterious SNPs on the human TERF1 protein triggering male infertility.

Published in:

Journal of Biomolecular Structure & Dynamics, 2023, v. 41, n. 24, p. 14665, doi. 10.1080/07391102.2023.2193995

By:

Harmak, Houda;
Redouane, Salaheddine;
Charoute, Hicham;
Aniq Filali, Ouafaa;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Computational study of the potential impact of AURKC missense SNPs on AURKC-INCENP interaction and their correlation to macrozoospermia.

Published in:

Journal of Biomolecular Structure & Dynamics, 2023, v. 41, n. 19, p. 9503, doi. 10.1080/07391102.2022.2142846

By:

Redouane, Salaheddine;
Charoute, Hicham;
Harmak, Houda;
Malki, Abderrahim;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article