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List of works by Linda Piekuse

Allelic variants of breast cancer susceptibility genes PALB2 and RECQL in the Latvian population

scientific article published on 03 July 2019

Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population.

scientific article published on 18 May 2016

Association between inherited monogenic liver disorders and chronic hepatitis C.

scientific article published on February 2014

Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia

scientific article published on 27 January 2018

Association of Variants in the CP, ATOX1 and COMMD1 Genes with Wilson Disease Symptoms in Latvia

scientific article published on 21 December 2019

Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin

scientific article published on 15 October 2011

Can a mother's polycystic ovary syndrome (PCOS)-related symptoms be used to predict the future clinical profile of PCOS in her adolescent daughter? A pilot study

scientific article published on 06 August 2020

Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome

article

Elevated serum levels of homocysteine as an early prognostic factor of psychiatric disorders in children and adolescents

scientific article published on October 2, 2012

Homocysteine and MTHFR C677T polymorphism in children and adolescents with psychotic and mood disorders.

scientific article published on 16 April 2013

Influence of IL15 gene variations on the clinical features, treatment response and risk of developing childhood acute lymphoblastic leukemia in Latvian population

scientific article published on 01 February 2018

Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism

article

Performance comparison of two whole genome amplification techniques in frame of multifactor preimplantation genetic testing.

scientific article

Reducing misdiagnosis caused by maternal cell contamination in genetic testing for early pregnancy loss

scientific article published on 15 October 2020

UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays

scientific article published on 06 March 2020

Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate

scientific article published on 01 April 2011