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The human WBSCR22 protein is involved in the biogenesis of the 40S ribosomal subunits in mammalian cells

PloS one, 2013-09, Vol.8 (9), p.e75686

2013

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EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Genome biology, 2013-01, Vol.14 (10), p.R120-R120

2013

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Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos

Human reproduction (Oxford), 2017-11, Vol.32 (11), p.2348-2357

2017

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Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy

Genome research, 2016-05, Vol.26 (5), p.567

2016

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Target prediction and validation of microRNAs expressed from FSHR and aromatase genes in human ovarian granulosa cells

Scientific reports, 2020-02, Vol.10 (1), p.2300-2300, Article 2300

2020

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Genome-wide histone modification profiling of inner cell mass and trophectoderm of bovine blastocysts by RAT-ChIP

PloS one, 2019-11, Vol.14 (11), p.e0225801-e0225801

2019

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Label-free, multiplexed detection of bacterial tmRNA using silicon photonic microring resonators

Biosensors & bioelectronics, 2012-06, Vol.36 (1), p.56-61

2012

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Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant

Gene, 2015-04, Vol.559 (2), p.144-148

2015

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A dual colour FISH method for routine validation of sexed Bos taurus semen

BMC veterinary research, 2019-04, Vol.15 (1), p.104-104, Article 104

2019

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FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation

Human molecular genetics, 2011-05, Vol.20 (10), p.1925-1936

2011

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Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays

Genome research, 1997-06, Vol.7 (6), p.606

1997

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Evaluating the Arrayed Primer Extension Resequencing Assay of TP53 Tumor Suppressor Gene

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (8), p.5503-5508

2002

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Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes

BMC biotechnology, 2011-02, Vol.11 (1), p.17-17, Article 17

2011

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Nucleic acid detection technologies and marker molecules in bacterial diagnostics

Expert review of molecular diagnostics, 2014-05, Vol.14 (4), p.489-500

2014

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Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides

BMC biotechnology, 2010-04, Vol.10 (1), p.34-34

2010

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Association study of 90 candidate gene polymorphisms in panic disorder

Psychiatric genetics, 2005-03, Vol.15 (1), p.17-24

2005

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Utilising FGF2, IGF2 and FSH in serum-free protocol for long-term in vitro cultivation of primary human granulosa cells

Molecular and cellular endocrinology, 2020-06, Vol.510, p.110816-110816, Article 110816

2020

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A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?

Developmental biology, 2019-03, Vol.447 (1), p.3-13

2019

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Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

BMC biotechnology, 2009-05, Vol.9 (1), p.45-45

2009

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In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

Nature medicine, 2019-11, Vol.25 (11), p.1699-1705

2019

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Nature (London), 2011-10, Vol.478 (7367), p.97-102

2011

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Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass

Fertility and sterility, 2018-06, Vol.109 (6), p.1127-1134.e1

2018

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Integrated carbon nanotube fibre–quartz tuning fork biosensor

Proceedings of the Estonian Academy of Sciences, 2012-01, Vol.61 (1), p.48

2012

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A patient with de novo 0.45Mb deletion of 2p16.1: The role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome

American journal of medical genetics. Part A, 2013-04, Vol.161 (4), p.865-870

2013

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The human WBSCR22 protein is involved in the biogenesis of the 40S ribosomal subunits in mammalian cells

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos

Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy

Target prediction and validation of microRNAs expressed from FSHR and aromatase genes in human ovarian granulosa cells

Genome-wide histone modification profiling of inner cell mass and trophectoderm of bovine blastocysts by RAT-ChIP

Label-free, multiplexed detection of bacterial tmRNA using silicon photonic microring resonators

Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant

A dual colour FISH method for routine validation of sexed Bos taurus semen

FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation

Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays

Evaluating the Arrayed Primer Extension Resequencing Assay of TP53 Tumor Suppressor Gene

Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes

Nucleic acid detection technologies and marker molecules in bacterial diagnostics

Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides

Association study of 90 candidate gene polymorphisms in panic disorder

Utilising FGF2, IGF2 and FSH in serum-free protocol for long-term in vitro cultivation of primary human granulosa cells

A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss

Integrated carbon nanotube fibre–quartz tuning fork biosensor

A patient with de novo 0.45Mb deletion of 2p16.1: The role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome

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