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Comprehensive molecular biomarker identification in breast cancer brain metastases

Journal of translational medicine, 2017-12, Vol.15 (1), p.269-269, Article 269

2017

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Ontology-based prediction of cancer driver genes

Scientific reports, 2019-11, Vol.9 (1), p.17405-9, Article 17405

2019

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Leptin Protein Expression and Promoter Methylation in Ovarian Cancer: A Strong Prognostic Value with Theranostic Promises

International journal of molecular sciences, 2021-11, Vol.22 (23), p.12872

2021

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Integration of Transcriptome and Metabolome Provides Unique Insights to Pathways Associated With Obese Breast Cancer Patients

Frontiers in oncology, 2020-05, Vol.10, p.804-804

2020

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MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia

BMC medical genetics, 2019-08, Vol.20 (1), p.144-144, Article 144

2019

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Prognostic value of HER2 status in bladder transitional cell carcinoma revealed by both IHC and BDISH techniques

BMC cancer, 2016-08, Vol.16 (1), p.653-653, Article 653

2016

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Prognostic value of TP53 expression and MGMT methylation in glioblastoma patients treated with temozolomide combined with other chemotherapies

Journal of neuro-oncology, 2021-05, Vol.152 (3), p.541-549

2021

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Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

American journal of human genetics, 2001-07, Vol.69 (1), p.49-54

2001

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A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members

Heliyon, 2021-05, Vol.7 (5), p.e06869, Article e06869

2021

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The Effect Sizes of PPARγ rs1801282 , FTO rs9939609, and MC4R rs2229616 Variants on Type 2 Diabetes Mellitus Risk among the Western Saudi Population: A Cross-Sectional Prospective Study

Genes, 2020-01, Vol.11 (1), p.98

2020

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Identification of 5 novel genes methylated in breast and other epithelial cancers

Molecular cancer, 2010-03, Vol.9 (1), p.51-51, Article 51

2010

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A genome-wide screen identifies frequently methylated genes in haematological and epithelial cancers

Molecular cancer, 2010-02, Vol.9 (1), p.44-44, Article 44

2010

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Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours

Oncogene, 2001-03, Vol.20 (12), p.1509-1518

2001

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The RASSF1A Tumor Suppressor Activates Bax via MOAP-1

The Journal of biological chemistry, 2006-02, Vol.281 (8), p.4557-4563

2006

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Frequent epigenetic inactivation of the SLIT2 gene in gliomas

Oncogene, 2003-07, Vol.22 (29), p.4611-4616

2003

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Prediction of Anti-Diabetic Drugs as Dual Inhibitors Against Acetylcholinesterase and Beta-Secretase: A Neuroinformatics Study

CNS & neurological disorders drug targets, 2016-01, Vol.15 (10), p.1216

2016

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A role for the RASSF1A tumor suppressor in the regulation of tubulin polymerization and genomic stability

Cancer research (Chicago, Ill.), 2004-06, Vol.64 (12), p.4244-4250

2004

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Frequent epigenetic inactivation of the SLIT2 gene in gliomas

Oncogene, 2003-07, Vol.22 (29), p.4611-4616

2003

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The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlights

BMC genomics, 2016-10, Vol.17 (Suppl 9), p.747-747, Article 747

2016

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Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes

Heliyon, 2020-11, Vol.6 (11), p.e05632-e05632, Article e05632

2020

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Involvement of the RASSF1A tumor suppressor gene in controlling cell migration

Cancer research (Chicago, Ill.), 2005-09, Vol.65 (17), p.7653-7659

2005

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Personalized medicine: a patient-centered paradigm

Journal of translational medicine, 2011-12, Vol.9 (1), p.206-206, Article 206

2011

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NORE1A, a homologue of RASSF1A tumour suppressor gene is inactivated in human cancers

Oncogene, 2003-02, Vol.22 (6), p.947-954

2003

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Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancers

Oncogene, 2003-03, Vol.22 (10), p.1580-1588

2003

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Depletion of the Ras association domain family 1, isoform A-Associated novel microtubule-associated protein, C19ORF5/MAP1S, causes mitotic abnormalities

Cancer research (Chicago, Ill.), 2007-01, Vol.67 (2), p.492-500

2007

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Comprehensive molecular biomarker identification in breast cancer brain metastases

Ontology-based prediction of cancer driver genes

Leptin Protein Expression and Promoter Methylation in Ovarian Cancer: A Strong Prognostic Value with Theranostic Promises

Integration of Transcriptome and Metabolome Provides Unique Insights to Pathways Associated With Obese Breast Cancer Patients

MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia

Prognostic value of HER2 status in bladder transitional cell carcinoma revealed by both IHC and BDISH techniques

Prognostic value of TP53 expression and MGMT methylation in glioblastoma patients treated with temozolomide combined with other chemotherapies

Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members

The Effect Sizes of PPARγ rs1801282 , FTO rs9939609, and MC4R rs2229616 Variants on Type 2 Diabetes Mellitus Risk among the Western Saudi Population: A Cross-Sectional Prospective Study

Identification of 5 novel genes methylated in breast and other epithelial cancers

A genome-wide screen identifies frequently methylated genes in haematological and epithelial cancers

Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours

The RASSF1A Tumor Suppressor Activates Bax via MOAP-1

Frequent epigenetic inactivation of the SLIT2 gene in gliomas

Prediction of Anti-Diabetic Drugs as Dual Inhibitors Against Acetylcholinesterase and Beta-Secretase: A Neuroinformatics Study

A role for the RASSF1A tumor suppressor in the regulation of tubulin polymerization and genomic stability

Frequent epigenetic inactivation of the SLIT2 gene in gliomas

The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlights

Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes

Involvement of the RASSF1A tumor suppressor gene in controlling cell migration

Personalized medicine: a patient-centered paradigm

NORE1A, a homologue of RASSF1A tumour suppressor gene is inactivated in human cancers

Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancers

Depletion of the Ras association domain family 1, isoform A-Associated novel microtubule-associated protein, C19ORF5/MAP1S, causes mitotic abnormalities

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