Lina Quteineh

Geneve, GE 1205, Switzerland

Last Updated: 09/26/2026

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Found 20 publications

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.

Journal: American journal of human genetics

Published: August 08, 2025

Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.

Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.

Journal: American journal of human genetics

Published: March 18, 2024

A case of nephrocalcinosis in a 7-month-old with congenital hypothyroidism: Insights from targeted exome sequencing.

A case of nephrocalcinosis in a 7-month-old with congenital hypothyroidism: Insights from targeted exome sequencing.

Journal: Pediatric discovery

Published: September 18, 2023

Substitution of arginine 219 by glycine compromises stability, dimerization, and catalytic activity in a G6PD mutant.

Substitution of arginine 219 by glycine compromises stability, dimerization, and catalytic activity in a G6PD mutant.

Journal: Communications biology

Published: August 07, 2023

Noninvasive prenatal diagnosis of Mendelian disorders for consanguineous couples by relative genotype dosage.

Noninvasive prenatal diagnosis of Mendelian disorders for consanguineous couples by relative genotype dosage.

Journal: Clinical genetics

Published: March 29, 2023

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.

Journal: American journal of human genetics

Published: May 27, 2022

Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.

Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.

Journal: Genes

Published: July 09, 2021

ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.

ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.

Journal: Clinical genetics

Published: April 17, 2021

Genetic immune and inflammatory markers associated with diabetes in solid organ transplant recipients.

Genetic immune and inflammatory markers associated with diabetes in solid organ transplant recipients.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: November 22, 2017

Association of variants in SH2B1 and RABEP1 with worsening of low-density lipoprotein and glucose parameters in patients treated with psychotropic drugs.

Association of variants in SH2B1 and RABEP1 with worsening of low-density lipoprotein and glucose parameters in patients treated with psychotropic drugs.

Journal: Gene

Published: December 15, 2016

Prediction of early weight gain during psychotropic treatment using a combinatorial model with clinical and genetic markers.

Prediction of early weight gain during psychotropic treatment using a combinatorial model with clinical and genetic markers.

Journal: Pharmacogenetics and genomics

Published: October 15, 2016

Genetic and clinic predictors of new onset diabetes mellitus after transplantation.

Genetic and clinic predictors of new onset diabetes mellitus after transplantation.

Journal: The pharmacogenomics journal

Published: September 15, 2016

Showing 1-12 of 20

Last Updated: 09/26/2026