Laurence-Moon-Biedl-Bardet syndrome in four kindreds

Combination of flow cytometry and functional imaging for monitoring of residual disease in myeloma.

Leukemia·2018

Investigating the feasibility of tumour molecular profiling in gastrointestinal malignancies in routine clinical practice.

Annals of oncology : official journal of the European Society for Medical Oncology·2018

Spatial genomic heterogeneity in multiple myeloma revealed by multi-region sequencing.

Nature communications·2017

Prediction of outcome in newly diagnosed myeloma: a meta-analysis of the molecular profiles of 1905 trial patients.

Leukemia·2017

Overexpression of EZH2 in multiple myeloma is associated with poor prognosis and dysregulation of cell cycle control.

Blood cancer journal·2017

Bi-allelic inactivation is more prevalent at relapse in multiple myeloma, identifying RB1 as an independent prognostic marker.

Blood cancer journal·2017

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Age at first sexual intercourse and frailty: Mendelian randomization and population-based evidence from NHANES and UK Biobank.

Sexual medicine·2026

Three-Year Experience of Cytogenetic and Molecular Genetic Evaluation in Patients With Disorders of Sex Development at a Tertiary Care Centre in Eastern India.

Cureus·2026

Two siblings with lipoid congenital adrenal hyperplasia: first reported case in Serbia and literature review.

Frontiers in endocrinology·2026

Comparative single-cell transcriptomics highlights species-biased developmental trajectories and candidate regulatory modules in primate spermatogenesis.

Reproductive biology·2026

Characteristics of Monozygotic Twins Discordant for Anorexia Nervosa: Comprehensive Risk Evaluation for Anorexia Nervosa in Twins (CREAT) Study.

European eating disorders review : the journal of the Eating Disorders Association·2026

Emerging molecular mechanisms of the ECM-exosome growth-plate axis in idiopathic short stature.

Frontiers in cell and developmental biology·2026

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Combination of flow cytometry and functional imaging for monitoring of residual disease in myeloma.

Investigating the feasibility of tumour molecular profiling in gastrointestinal malignancies in routine clinical practice.

Spatial genomic heterogeneity in multiple myeloma revealed by multi-region sequencing.

Prediction of outcome in newly diagnosed myeloma: a meta-analysis of the molecular profiles of 1905 trial patients.

Overexpression of EZH2 in multiple myeloma is associated with poor prognosis and dysregulation of cell cycle control.

Bi-allelic inactivation is more prevalent at relapse in multiple myeloma, identifying RB1 as an independent prognostic marker.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Age at first sexual intercourse and frailty: Mendelian randomization and population-based evidence from NHANES and UK Biobank.

Three-Year Experience of Cytogenetic and Molecular Genetic Evaluation in Patients With Disorders of Sex Development at a Tertiary Care Centre in Eastern India.

Two siblings with lipoid congenital adrenal hyperplasia: first reported case in Serbia and literature review.

Comparative single-cell transcriptomics highlights species-biased developmental trajectories and candidate regulatory modules in primate spermatogenesis.

Characteristics of Monozygotic Twins Discordant for Anorexia Nervosa: Comprehensive Risk Evaluation for Anorexia Nervosa in Twins (CREAT) Study.

Emerging molecular mechanisms of the ECM-exosome growth-plate axis in idiopathic short stature.

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