Sigri Beckers

Edegem, VLG 2650, Belgium

Last Updated: 09/26/2026

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Found 31 publications

Rare Heterozygous PCSK1 Variants in Human Obesity: The Contribution of the p.Y181H Variant and a Literature Review.

Rare Heterozygous PCSK1 Variants in Human Obesity: The Contribution of the p.Y181H Variant and a Literature Review.

Journal: Genes
Published: June 24, 2022

Nonmosaic Isodicentric Y Chromosome: A Rare Cause of Azoospermia- From Genetics to Clinical Practice.

Nonmosaic Isodicentric Y Chromosome: A Rare Cause of Azoospermia- From Genetics to Clinical Practice.

Journal: Case reports in endocrinology
Published: March 31, 2020

Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene (SERPING1).

Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene (SERPING1).

Journal: The journal of allergy and clinical immunology. In practice
Published: July 19, 2018

Evaluation of a Role for NPY and NPY2R in the Pathogenesis of Obesity by Mutation and Copy Number Variation Analysis in Obese Children and Adolescents.

Evaluation of a Role for NPY and NPY2R in the Pathogenesis of Obesity by Mutation and Copy Number Variation Analysis in Obese Children and Adolescents.

Journal: Annals of human genetics
Published: March 16, 2017

Thoracic dimples and dysmorphic features associated with a partial duplication and triplication of chromosome 12q24.

Thoracic dimples and dysmorphic features associated with a partial duplication and triplication of chromosome 12q24.

Journal: Clinical dysmorphology
Published: August 09, 2016

Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal test.

Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal test.

Journal: Prenatal diagnosis
Published: January 13, 2016

Screening for rare variants in the PNPLA3 gene in obese liver biopsy patients.

Screening for rare variants in the PNPLA3 gene in obese liver biopsy patients.

Journal: Clinics and research in hepatology and gastroenterology
Published: December 10, 2015

Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients.

Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients.

Journal: Molecular genetics and metabolism
Published: November 24, 2015

CNV analysis and mutation screening indicate an important role for the NPY4R gene in human obesity.

CNV analysis and mutation screening indicate an important role for the NPY4R gene in human obesity.

Journal: Obesity (Silver Spring, Md.)
Published: July 29, 2015

Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity.

Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity.

Journal: Endocrine
Published: July 27, 2015

Nucleotide variation of sFRP5 gene is not associated with obesity in children and adolescents.

Nucleotide variation of sFRP5 gene is not associated with obesity in children and adolescents.

Journal: Molecular biology reports
Published: July 14, 2015

Association study of PNPLA2 gene with histological parameters of NAFLD in an obese population.

Association study of PNPLA2 gene with histological parameters of NAFLD in an obese population.

Journal: Clinics and research in hepatology and gastroenterology
Published: June 25, 2015
Showing 1-12 of 31

Last Updated: 09/26/2026