List of works - Laura Turpín-Fenoll

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population.

scientific article

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.

scientific article published on 16 October 2017

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

scientific article published on 10 January 2013

Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome.

scientific article

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

scientific article published on 12 February 2016

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome.

scientific article

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

scientific article

MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis

scientific article published on 31 July 2013

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.

scientific article

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

scientific article

Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

scientific article published on 10 October 2014

Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

scientific article published on 21 November 2020

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

scientific article

The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

scientific article published on 22 December 2013

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

scientific article published on 11 November 2016

Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis

scientific article

List of works by Laura Turpín-Fenoll

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population.

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome.

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome.

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis