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List of works by Maris Laan

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Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1.

scientific article published on 23 July 2007
Extensive load of somatic CNVs in the human placenta

scientific article published on 10 February 2015
Increased placental expression and maternal serum levels of apoptosis-inducing TRAIL in recurrent miscarriage

scientific article published on 3 January 2013
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia

scientific article published on 01 August 2018
RNA sequencing of chorionic villi from recurrent pregnancy loss patients reveals impaired function of basic nuclear and cellular machinery

scientific article published on 08 December 2016
High divergence in primate-specific duplicated regions: human and chimpanzee chorionic gonadotropin beta genes

scientific article
N-acetyltransferase 8, a positional candidate for blood pressure and renal regulation: resequencing, association and in silico study

scientific article
Structural genomic variation as risk factor for idiopathic recurrent miscarriage

scientific article
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

scientific article published in Nature Communications
The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22.

scientific article
Effects of RNA integrity on transcript quantification by total RNA sequencing of clinically collected human placental samples

scientific article published on 26 April 2017
Human CuZn superoxide dismutase enzymatic activity in cells is regulated by the length of the mRNA.

scientific article published on April 1995
Developmental programming of growth: genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination

scientific article published on 29 August 2013
Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits

scientific article
The human ribosomal protein S7-encoding gene: isolation, structure and localization in 2p25

scientific article
Putative predictors of antibodies against follicle-stimulating hormone in female infertility: a study based on in vitro fertilization patients

scientific article published in March 2007
A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage

scientific article published on 15 March 2013
FSHB −211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women

article
Structural and functional analysis of rare missense mutations in human chorionic gonadotrophin β-subunit

scientific article
No evidence of somatic DNA copy number alterations in eutopic and ectopic endometrial tissue in endometriosis

scientific article
A novel snoRNA (U73) is encoded within the introns of the human and mouse ribosomal protein S3a genes

scientific article
Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy number

article
Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families

scientific article published on 27 March 2017
Annexin A5 Promoter Haplotype M2 Is Not a Risk Factor for Recurrent Pregnancy Loss in Northern Europe

scientific article published on 2 July 2015
The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young men.

scientific article published on 23 March 2017
Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators

scientific article published on 07 September 2016
Subsequent Event Risk in Individuals With Established Coronary Heart Disease

scientific article published on 21 March 2019
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

scientific article published on 21 March 2019
The Visual Assignment of Genes by Fiber-Fish: BTF3 Protein Homologue Gene (BTF3) and a Novel Pseudogene of Human RNA Helicase A (DDX9P) on 13q22

article
Haplotype phasing and inheritance of copy number variants in nuclear families

scientific article published on 8 April 2015
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019
HYPEST study: profile of hypertensive patients in Estonia

scientific article published on August 31, 2011
'Carriers of variant luteinizing hormone (V-LH) among 1593 Baltic men have significantly higher serum LH'

scientific article published on 26 March 2015
The Effect of Genetic Variation on the Placental Transcriptome in Humans.

scientific article
Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives

scientific article published on 18 January 2020
Parent-of-origin-specific allelic expression in the human placenta is limited to established imprinted loci and it is stably maintained across pregnancy

scientific article published on 26 June 2019
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics
Genetics of Sex Hormone-Binding Globulin and Testosterone Levels in Fertile and Infertile Men of Reproductive Age.

scientific article published on 11 April 2017
Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019
Response to "Annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?".

scientific article
NR5A1 c.991-1G > C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance

scientific article published on 09 December 2020
185-POS

scholarly article by Kristiina Rull et al published January 2015 in Pregnancy hypertension
WITHDRAWN: TNF-Related Apoptosis-Inducing Ligand TRAIL as a Potential Biomarker for Early Pregnancy Complications

retracted scientific article published on 14 June 2012
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

scientific article published on 30 April 2024
Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome

scientific article published on 01 August 2019
Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020
Systematic review of the monogenetic causes of male infertility: the first step towards diagnostic gene panels in the andrology clinic

scientific article published on 01 May 2019

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