Caroline Benech

Brest, France

Last Updated: 09/26/2026

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Found 26 publications

Identification of the novel c.149-8C>G splicing variant in RHCE*02 that weakens C antigen expression.

Identification of the novel c.149-8C>G splicing variant in RHCE*02 that weakens C antigen expression.

Journal: Transfusion

Published: February 05, 2026

Investigating the molecular basis of the serological Rh D-negative phenotype in Indonesia: nature, frequency, and impact for diagnostics.

Investigating the molecular basis of the serological Rh D-negative phenotype in Indonesia: nature, frequency, and impact for diagnostics.

Journal: Transfusion

Published: January 21, 2026

A novel JK-null allele due to splicing variant.

A novel JK-null allele due to splicing variant.

Journal: Transfusion

Published: January 20, 2026

Functional investigation of the RHD gene promoter: Molecular changes are rarely responsible for variant D phenotype in Thai donors.

Functional investigation of the RHD gene promoter: Molecular changes are rarely responsible for variant D phenotype in Thai donors.

Journal: Transfusion

Published: September 11, 2025

A novel RHCE*ce(c.48C)-D(4)-ce allele in a family of African ancestry.

A novel RHCE*ce(c.48C)-D(4)-ce allele in a family of African ancestry.

Journal: Transfusion

Published: August 29, 2025

The novel JK*02(588G;929G) allele in an Indian patient dramatically impairs the expression of the Jkb antigen.

The novel JK*02(588G;929G) allele in an Indian patient dramatically impairs the expression of the Jkb antigen.

Journal: Transfusion

Published: February 19, 2025

Alloanti-D in a DBT pregnant woman responsible for hemolytic disease of the fetus and newborn: Molecular study and genetic counseling.

Alloanti-D in a DBT pregnant woman responsible for hemolytic disease of the fetus and newborn: Molecular study and genetic counseling.

Journal: Transfusion

Published: January 23, 2025

Combining computational approaches and functional analysis for characterizing the deleterious effect of RHD gene variants on splicing in the Chinese population.

Combining computational approaches and functional analysis for characterizing the deleterious effect of RHD gene variants on splicing in the Chinese population.

Journal: Transfusion

Published: October 10, 2024

An unusual diagnosis of alpha-mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation.

An unusual diagnosis of alpha-mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation.

Journal: American journal of medical genetics. Part A

Published: October 10, 2023

First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.

First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.

Journal: Blood transfusion = Trasfusione del sangue

Published: September 26, 2023

3q29 duplications: A cohort of 46 patients and a literature review.

3q29 duplications: A cohort of 46 patients and a literature review.

Journal: American journal of medical genetics. Part A

Published: September 20, 2023

Anti-D alloimmunization by Asia type DEL red blood cell units in a D-negative Thai patient.

Anti-D alloimmunization by Asia type DEL red blood cell units in a D-negative Thai patient.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: March 21, 2023

Showing 1-12 of 26

Last Updated: 09/26/2026