Gerard Tachdjian

Clamart, France

Last Updated: 09/26/2026

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Found 53 publications

Genetic testing for oocyte donor candidates: time for an international recommendation?

Genetic testing for oocyte donor candidates: time for an international recommendation?

Journal: Fertility and sterility

Published: June 06, 2025

Six New Cases of 22q13.2 Gain Including TFC20: First Report of Triplication and Smallest Duplication Associated With Neurodevelopmental Delays.

Six New Cases of 22q13.2 Gain Including TFC20: First Report of Triplication and Smallest Duplication Associated With Neurodevelopmental Delays.

Journal: Clinical genetics

Published: February 02, 2025

Improved functionality of hepatic spheroids cultured in acoustic levitation compared to existing 2D and 3D models.

Improved functionality of hepatic spheroids cultured in acoustic levitation compared to existing 2D and 3D models.

Journal: Scientific reports

Published: June 03, 2024

Chromosomal abnormalities in oocyte donor candidates: a French survey of over 8,200 karyotypes.

Chromosomal abnormalities in oocyte donor candidates: a French survey of over 8,200 karyotypes.

Journal: Fertility and sterility

Published: February 26, 2024

Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene.

Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene.

Journal: Stem cell research

Published: January 15, 2024

KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomas.

KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomas.

Journal: European journal of endocrinology

Published: November 01, 2023

Critical contribution of mitochondria in the development of cardiomyopathy linked to desmin mutation.

Critical contribution of mitochondria in the development of cardiomyopathy linked to desmin mutation.

Journal: Stem cell research & therapy

Published: October 03, 2023

An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14.

An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14.

Journal: Neuromuscular disorders : NMD

Published: June 22, 2023

Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic hernia.

Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic hernia.

Journal: Prenatal diagnosis

Published: June 17, 2022

Stepwise GATA1 and SMC3 mutations alter megakaryocyte differentiation in a Down syndrome leukemia model.

Stepwise GATA1 and SMC3 mutations alter megakaryocyte differentiation in a Down syndrome leukemia model.

Journal: The Journal of clinical investigation

Published: November 01, 2021

First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15.

First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15.

Journal: Taiwanese journal of obstetrics & gynecology

Published: July 19, 2021

Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort study.

Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort study.

Journal: The lancet. Diabetes & endocrinology

Published: June 26, 2021

Showing 1-12 of 53

Last Updated: 09/26/2026