Works matching IS 11108630 AND DT 2025 AND VI 26 AND IP 1

Results: 73

Association of CCR2 and AGT gene variants with lipid profiles and cardiovascular risk factors in coronary artery disease patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00705-8

By:

Eba, Ale;
Raza, Syed Tasleem;
Ahmad, Bashir;
Afreen, Sheeba;
Srivastava, Sanchita;
Mahdi, Farzana;
Nag, Riya

Publication type:

Article

Genetic insights from whole-exome sequencing in Moroccan patients with non-small cell lung cancer: a case report.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00698-4

By:

Fakhkhari, Meryem;
Vinu, Manikandan;
Chaibi, Houda;
Dieng, Mame Massar;
Chebak, Meryem;
Hajjout, Khadija;
Zahraoui, Rachida;
Bouyahyaoui, Nawal;
Bourkadi, Jamal-Eddine;
Idaghdour, Youssef;
Sadki, Khalid

Publication type:

Article

Genetic association of toll like receptors and breast cancer: a novel approach toward countering the breast cancer tumor invasiveness and recurrence.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00706-7

By:

Das, Avishek;
Banerjee, Avisek

Publication type:

Article

A novel noncanonical splicing pathogenic variant in PAX3 associated with Waardenburg Syndrome type 1 in an Iranian family.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00652-4

By:

Soosanabadi, Mohsen;
Biglari, Sajjad;
Bayat, Sahar;
Ghorashi, Tahereh;
Sohanforooshan Moghaddam, Atefeh;
Gholami, Milad

Publication type:

Article

Identification of high confidence genes involved in the manifestation of ventricular septal defect.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00708-5

By:

Shanthithadda, Chaithra;
Ramachandra, Nallur Basappa

Publication type:

Article

Prenatal diagnosis of a rare 1p36 heterochromatin variation with a ventricular septal defect in a twin pregnancy.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00691-x

By:

Wei, Xingye;
Zhang, Pingping;
Shi, Xuedong;
Wang, Fangna;
Sun, Yanmei

Publication type:

Article

Exploration of the genetic and environmental determinants of male infertility: a comprehensive review.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00703-w

By:

Imran, Muhammad;
Zia, Ramna;
Arshad, Muneeb;
Fayyaz, Fatima;
Haider, Tauseef;
Tabraiz, Ali;
Arshad, Iqra;
Sharif, Muhammad Anees;
Javed, Benish

Publication type:

Article

SARE: an optimized method for detection functional regulatory elements in genome.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00695-7

By:

Hosseinpoor, Mohammadjavad

Publication type:

Article

Unraveling the roles of BMS1, ZNF749 and miR-6726-5p in MODS progression via integrated multiomics and ML-based approach.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00697-5

By:

Mathur, Dhairya;
Beg, Anam;
K., Sajani;
Husain, Syed Asif;
Singh, Prithvi

Publication type:

Article

Molecular mavericks: unveiling the matrix metalloproteinase gene's role in ovarian cancer.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00693-9

By:

Bindhu, Devi Krishna Ratnakaran;
Murugan, Lavanya;
Mathews, Sneha Grace;
Krishnamurty, Nandini;
Murali, Sanjana;
Agarwal, Preet;
Junieus, Elizabeth Rani;
Francis, Andrea Mary

Publication type:

Article

Classification of patients with lithium-treated bipolar disorder based on gene expression: Dirichlet Bayesian network model.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00690-y

By:

Salari, Nader;
Pilangorgi, Sahar Souri;
Almasi, Afshin;
Shahsavari, Soodeh;
Fournier, Andrew J.

Publication type:

Article

Towards personalized prostate cancer treatment with docetaxel in indonesia: a pharmacogenomics perspective.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00702-x

By:

Malau, Jekmal;
Rohmah, Siti;
Meilani, Nanda Diva;
Hermosaningtyas, Anastasia Aliesa;
Kasasiah, Ahsanal;
Rahmasari, Ratika;
Setiawan, Heri;
Hasby, Fahri Azhari;
Raekiansyah, Muhareva;
Manalu, Rosario Trijuliamos

Publication type:

Article

Timing of gene expression alters susceptibility to aflatoxicosis: a heterogeneous spectrum of disease in response to a single universal agent.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00699-3

By:

Kotb, Magd Ahmed;
Lotfi, Nabil Mohamed Amr;
Elhatw, Ahmed Khaled

Publication type:

Article

Association of tumour necrosis factor-alpha (rs1800629 and rs361525) gene polymorphisms with tuberculosis susceptibility: a meta-analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00692-w

By:

Jayakumar, V.;
Nishmaa, S.;
Lakshmi, K.

Publication type:

Article

Genetic and infectious determinants of puerperal fever: a study of viral and bacterial coinfections in postpartum women.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00696-6

By:

Olaniyan, Mathew Folaranmi;
Odegbemi, Odekunle Bola;
Tijani, Wakili Adelani;
Olaniyan, Tolulope Busayo;
Adeniran, Medinat Taiwo;
Oniye, Adesola Helen;
Adesina, Opeyemi Olufeyisola;
Adejumo, Babatunde Ishola Gabriel;
Ajiboye, Kemi Felicia;
Mohammed, Ahmadu Shehu;
Adeboye, Olubunmi Omotola Moses

Publication type:

Article

Genetic and phenotypic characteristics of 3 patients with limb-girdle muscular dystrophy: experience in a medical center in Mexico.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00685-9

By:

Martínez-Montoya, Valentina;
Martínez-Herrera, Alejandro;
Mancera-Páez, Oscar;
Hidalgo-Bravo, Alberto;
Rivera-Vega, María R.

Publication type:

Article

Epigenetic factors in posttraumatic stress disorder resilience and susceptibility.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00684-w

By:

Addissouky, Tamer A.;
El Tantawy El Sayed, Ibrahim;
Wang, Yuliang

Publication type:

Article

Investigation of rs328 polymorphism of lipoprotein lipase and rs1260326 polymorphism of glucokinase regulatory genes in individuals with type 2 diabetes in Yazd, Iran.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00682-y

By:

Rezazadeh Khabaz, Mohammad Javad;
Dastghaib, Sanaz;
Vahidi Mehrjardi, Mohammad Yahya;
Sheikhha, Mohammad Hasan

Publication type:

Article

Genetic counselling of disorders of sex development (DSD) in low middle income country (LMIC): case studies.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00681-z

By:

Faradz, Sultana;
Maritska, Ziske;
Komandur, Sreelatha;
Hasan, Qurratulain Annie

Publication type:

Article

A comprehensive in silico investigation unravels the structural and functional consequences of non-synonymous single-nucleotide polymorphisms in human OXTR gene.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00680-0

By:

Mazumder, Puja;
Das, Shuvo Chandra;
Mondol, Sobuj;
Afif, Ibrahim Khalil;
Howlader, Mithu;
Gupta, Shipan Das;
Hossain, Md. Murad;
Rahman, Md. Mijanur

Publication type:

Article

Case report: dual diagnosis of Mulibrey nanism and Jacobs syndrome in an Indian boy.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00694-8

By:

Kumari, Pritti;
Aggarwal, Rohina;
Valodara, Akshi;
Patel, Hetvi;
Dhoriya, Dipak;
Suthar, Ankita;
Aggarwal, Somesh

Publication type:

Article

Innovative gene therapy strategies for tackling obesity.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00686-8

By:

Sheikh-Hosseini, Motahareh;
Moarefzadeh, Mohammad;
Alsaedi, Alyaa Abdulhussein;
Amshawee, Ahmed M.;
Al-Mozani, Sahar Kareem;
Abed, Ahmed Yaseen;
Neissi, Mostafa;
Roudsari, Peyvand Parhizkar

Publication type:

Article

Relapse-specific genetic patterns in the exomic mutational landscape in acute myeloid leukemia.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00688-6

By:

Qureshi, Wardah;
Jamal, Aisha;
Gohar, Atia;
Mansuri, Marium Imran;
Irfan, Muhammad;
Khan, Ishtiaq Ahmad;
Shakeel, Muhammad

Publication type:

Article

Immunogenetic variations in HIV serotypes in patients attending military hospital, Warri, Nigeria.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00683-x

By:

Olaniyan, Mathew Folaranmi;
Omosigho, Pius Omoruyi;
Uwaifo, Ferdinand;
Olaniyan, Tolulope Busayo;
Adepoju, Ademola Lukman;
Odegbemi, Odekunle Bola

Publication type:

Article

Investigating the expression level of 9-methylated septin 9 in different grades of colorectal cancer—a meta-analysis study.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00666-y

By:

Mohandesi khosrosroshahi, Elaheh;
Bashi Zadeh Fakhar, Haniyeh;
Akbari, Mohammad-Esmaiel;
Izadi, Neda

Publication type:

Article

Identification of key genes and signaling pathway in the pathogenesis of Huntington's disease via bioinformatics and next generation sequencing data analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00660-4

By:

Vastrad, Basavaraj;
Vastrad, Chanabasayya

Publication type:

Article

Genetic screening of malay familial hypercholesterolemia patient for LDLRAP1/PCSK9/APOB mutations via whole exome sequencing.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00673-z

By:

Abdullah-Zawawi, Muhammad-Redha;
Mohd Rani, Zam Zureena;
Seeni Ahamed Mydeen, Nur Syakeera;
Mohd Yunos, Ryia Illani;
Sulaiman, Siti Aishah;
Badaruddin, Izzatul 'Aliaa;
Ismet, Rose;
Mustafa, Norlaila;
Abu Zahid, Syahidatun Najwa;
Jamal, Rahman;
Hamzah, Azrul Azlan;
Abdul Murad, Nor Azian

Publication type:

Article

Correction: Association of VEGF promoter polymorphisms with gastrointestinal tract cancer risk and therapy response: a systematic review.

Published in:

2025

By:

Mahajan, Deepanshi;
Sambyal, Vasudha;
Guleria, Kamlesh

Publication type:

Correction Notice

Apoptotic effects of crude muscle extract from marine pufferfish Chelonodon patoca against human cancer cell lines.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00667-x

By:

Sekar, Niranjni;
Valayapathi, Rajasekar;
Azhagudurai, Aarthi;
Durai, Prabhu;
Selvakumar, Shiva Shakthi;
Chinnasamy, Arulvasu

Publication type:

Article

The role of non-coding RNAs (ncRNAs) and their potential connection with cancer.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00689-5

By:

Absalan, Safura;
Vaziri, Hamidreza

Publication type:

Article

ceRNA networks in ischemic stroke: a bibliometric analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00687-7

By:

Wei, Loo Keat;
Griffiths, Lyn R.;
Tollefsbol, Trygve O.

Publication type:

Article

Association of estrogen receptor alpha gene PvuII and XbaI polymorphisms with obesity-related phenotypes and body composition in Iranian children and adolescents: a cross-sectional study.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00678-8

By:

Montazeri-Najafabady, Nima;
Dabbaghmanesh, Mohammad Hossein

Publication type:

Article

The relationship between p53 and the malignant transformation of nasal inverted papilloma: a meta-analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00677-9

By:

Zhan, Hao;
Sun, Bo;
Jiang, Xijiao;
Zhang, Farong;
Wang, Wuchen;
Luo, Yong

Publication type:

Article

Biochemical and genetic studies on type 2 diabetes mellitus subjects of Ekiti State, Nigeria: Association between CAPN10 and Diabetes: D. O. Adebo.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00676-w

By:

Adebo, David O.;
Olaniyan, Mathew F.;
Daramola, Gabriel O.;
Ugege, Christian O.;
Odegbemi, Odekunle B.

Publication type:

Article

Management of mucopolysaccharidosis type I using enzyme replacement therapy: Egyptian experience: ERT in MPS type I.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00668-w

By:

Fateen, Ekram;
Sahrigy, Sally A. F. El;
Ibrahim, Mona;
Elhossini, Rasha M.;
Ahmed, Hoda H.;
Esmail, Asmaa;
Radwan, Amira;
Salama, Iman Ibrahim;
ElBaky, Abeer M. NourElDin Abd;
Ezzeldin, Nada;
Rahman, Azza M. O. Abdel;
Aglan, Mona

Publication type:

Article

Insights on 7p21 deletion including the TWIST1 gene: a case report of an adult patient with macroglossia and a literature review.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00674-y

By:

Peker, Alp;
Clark, Özden Altıok;
Coşkun, Mert;
Duru, Ali;
Yalabık, Feyza Altunbaş;
Aracı, Duygu Gamze;
Toylu, Aslı;
Uzuner, Sezin Yakut;
Derin, Alper Tunga;
Mıhçı, Ercan

Publication type:

Article

Unraveling the role of NOG gene in hereditary sensory neuropathy type 1F through CRISPR/Cas9-mediated ATL3 knockout.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00672-0

By:

Saffar, Mahsa;
Dara, Mahintaj;
Fazelzadeh Haghighi, Maryam;
Baneshi, Maryam;
Tabei, Seyed Mohammad Bagher

Publication type:

Article

Blood group diversity in Borneo.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00664-0

By:

Assyuhada, Mat Ghani Siti Nor;
Hajar, Che Ghazali Norul;
'Adani, Sanusi Nurul;
Hassan, Mohd Nazri;
Mohammad Isa, Nilie Syamila;
Ali, Nur Saiyidah Hanisah;
Mohamad, Siti Aisyah;
Aziz, Mohd Yusmaidie;
Furqoni, Abdul Hadi;
Chambers, Geoffrey Keith;
Zulkafli, Zefarina;
Edinur, Hisham Atan

Publication type:

Article

lncRNA FLVCR1-AS1 sponges miR-381-3p and promotes Wnt signaling pathway resulting in colorectal cancer progression.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00663-1

By:

Ahmadi Beni, Faeze;
Abdolvand, Mohammad;
poorbafrani, Fariborz;
Salehi, Mansoor;
Dehghanian, Fariba;
Kazemi, Mohammad

Publication type:

Article

Adoptive transfer of natural killer cells in therapeutic treatment of COVID-19 patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00670-2

By:

Alamri, Abdulaziz

Publication type:

Article

Evaluation of pathogenic variant in WFS1 in a patient with Wolfram syndrome.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00657-z

By:

Hoseinzadeh, Marziyeh;
Jahani, Mohammad Mehdi;
Nasrniya, Samane;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Unraveling the structural and functional consequences of non-synonymous single-nucleotide polymorphisms (nsSNPs) in human SOCS2: an in silico approach.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00669-9

By:

Hossain, Tanvir;
Islam, Md. Nur;
Hossain, Md. Anwar;
Rahman, Md. Mofizur;
Islam, Mohammed Mafizul;
Gupta, Shipan Das

Publication type:

Article

Assessing the association of rare MDR1 variants (rs944806668, rs1816042256, and rs1295312177) with steroid response in Iraqi children with idiopathic nephrotic syndrome.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00662-2

By:

Abd Alridha, Ali Mohammed;
Kadhim, Dheyaa Jabbar;
Alkhazrajy, Ayad Hussein Ali

Publication type:

Article

Whole-exome sequencing and molecular dynamics confirm pathogenicity of a novel SLC6A6 mutation in Leber congenital amaurosis.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00659-x

By:

Natarajan, Srikrupa N.;
Ansar, Samdani;
Sripriya, Sarangapani;
Parveen, Sen;
Gupta, Ravi;
Vetrivel, Umashankar;
Sinnakarupan, Mathavan

Publication type:

Article

Unveiling the association between long non-coding RNAs (RP5-833A20.1, DYNLRB2-2, and APOA1-AS) and ischemic stroke: exploring biomarkers, and clinical implications: Expression of RP5-833A20.1, DYNL RB2-2, and APOA1 antisense after ischemic stroke: M. Bayat et al.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00658-y

By:

Bayat, Mahnaz;
Mokhtari, Mahsa;
Mokhtari, Mohammad Javad;
Gharbi, Negin;
Tabrizi, Reza;
Salehi, Mohammad Saied;
Karimi, Najmeh;
Rahimi, Moosa;
Hooshmandi, Etrat;
Zafarmand, Seyedeh Shaghayegh;
Owjfard, Maryam;
Lashanizadegan, Ramin;
Dara, Mahintaj;
Borhani-Haghighi, Afshin

Publication type:

Article

FOXF2 rs41300825 and NOTCH3 rs1043994 as risk loci for cerebral small vessel disease in Egyptian ischemic stroke patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00641-7

By:

Hussein, Fatma Salama;
Sayed, Soha Saad Eldin;
Mohammed, Hossam Shokri;
Kamal, Maha Moustafa

Publication type:

Article

Exploring the effects of alpha-pinene on apoptosis induction in human colon cancer cells via the PI3K/AKT signaling pathway: an in vitro study.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00656-0

By:

Shafieipour, Sara;
Zamanian, Yasaman;
Hadipour, Elham;
Sinaei, Reza;
Khoshnazar, Seyedeh Mahdieh

Publication type:

Article

Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00653-3

By:

Soeroso, Noni Novisari;
Zain-Hamid, Rozaimah;
Bihar, Syamsul;
Soliha, Chaliza;
Ananda, Fannie Rizki;
Aida

Publication type:

Article

Association between CAPN-10 gene variant and diabetes mellitus in Nigeria: a review.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00655-1

By:

Adebo, David Olufemi;
Olaniyan, Mathew Folaranmi;
Ugege, Christian Onosetale;
Odegbemi, Odekunle Bola

Publication type:

Article

Case report: identification of novel variant in SLC26A2 gene and preimplantation genetic testing for monogenic disorders in preventing diastrophic dysplasia.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00649-z

By:

Tonyan, Ziravard N.;
Nasykhova, Yulia A.;
Danilova, Maria M.;
Shabanova, Elena S.;
Bespalova, Olesya N.;
Kogan, Igor Y.;
Glotov, Andrey S.

Publication type:

Article