Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods

por Yoshihara, Masahito, Kere, Juha
Publicado 2023

SAMstrt: statistical test for differential expression in single-cell transcriptome with spike-in normalization

por Katayama, Shintaro, Töhönen, Virpi, Linnarsson, Sten, Kere, Juha
Publicado 2013

Identification of Novel Transcribed Regions in Zebrafish (Danio rerio) Using RNA-Sequencing

por Wang, Jingwen, Vesterlund, Liselotte, Kere, Juha, Jiao, Hong
Publicado 2016

Idiopathic scoliosis: a systematic review and meta-analysis of heritability

por Cheng, Tian, Einarsdottir, Elisabet, Kere, Juha, Gerdhem, Paul
Publicado 2022

Genetic evidence of multiple loci in dystocia - difficult labour

por Algovik, Michael, Kivinen, Katja, Peterson, Hanna, Westgren, Magnus, Kere, Juha
Publicado 2010

The zebrafish transcriptome during early development

por Vesterlund, Liselotte, Jiao, Hong, Unneberg, Per, Hovatta, Outi, Kere, Juha
Publicado 2011

Computational approach to evaluate scRNA-seq data quality and gene body coverage with SkewC

por Abugessaisa, Imad, Hasegawa, Akira, Katayama, Shintaro, Kere, Juha, Kasukawa, Takeya
Publicado 2023

The Zebrafish Orthologue of the Dyslexia Candidate Gene DYX1C1 Is Essential for Cilia Growth and Function

por Chandrasekar, Gayathri, Vesterlund, Liselotte, Hultenby, Kjell, Tapia-Páez, Isabel, Kere, Juha
Publicado 2013

Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes

por Lindberg, Eva, Moller, Claes, Kere, Juha, Wedenoja, Satu, Anderzén-Carlsson, Agneta
Publicado 2020

Corrigendum: Gene expression profiling of pre-eclamptic placentae by RNA sequencing

por Kaartokallio, Tea, Cervera, Alejandra, Kyllönen, Anjuska, Laivuori, Krista, Kere, Juha, Laivuori, Hannele
Publicado 2016

Discovering heritable modes of MEG spectral power

por Leppäaho, Eemeli, Renvall, Hanna, Salmela, Elina, Kere, Juha, Salmelin, Riitta, Kaski, Samuel
Publicado 2019

Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods

por Katayama, Shintaro, Skoog, Tiina, Söderhäll, Cilla, Einarsdottir, Elisabet, Krjutškov, Kaarel, Kere, Juha
Publicado 2019

Embryonic LTR retrotransposons supply promoter modules to somatic tissues

por Hashimoto, Kosuke, Jouhilahti, Eeva-Mari, Töhönen, Virpi, Carninci, Piero, Kere, Juha, Katayama, Shintaro
Publicado 2021

Expression Analysis of the NLRP Gene Family Suggests a Role in Human Preimplantation Development

por Zhang, Pu, Dixon, Morag, Zucchelli, Marco, Hambiliki, Fredwell, Levkov, Lev, Hovatta, Outi, Kere, Juha
Publicado 2008

aThe dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer

por Rosin, Gustaf, Hannelius, Ulf, Lindström, Linda, Hall, Per, Bergh, Jonas, Hartman, Johan, Kere, Juha
Publicado 2012

Cohort profile: the Finnish Genetics of Pre-eclampsia Consortium (FINNPEC)

por Jääskeläinen, Tiina, Heinonen, Seppo, Kajantie, Eero, Kere, Juha, Kivinen, Katja, Pouta, Anneli, Laivuori, Hannele
Publicado 2016

A preliminary transcriptome analysis suggests a transitory effect of vitamin D on mitochondrial function in obese young Finnish subjects

por Einarsdottir, Elisabet, Pekkinen, Minna, Krjutškov, Kaarel, Katayama, Shintaro, Kere, Juha, Mäkitie, Outi, Viljakainen, Heli
Publicado 2019

Generation of RNA sequencing libraries for transcriptome analysis of globin-rich tissues of the domestic dog

por Ezer, Sini, Yoshihara, Masahito, Katayama, Shintaro, Daub, Carsten, Lohi, Hannes, Krjutskov, Kaarel, Kere, Juha
Publicado 2021

Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2

por Bieder, Andrea, Chandrasekar, Gayathri, Wason, Arpit, Erkelenz, Steffen, Gopalakrishnan, Jay, Kere, Juha, Tapia-Páez, Isabel
Publicado 2023

CRISPR/Cas9-mediated activation of NR5A1 steers female human embryonic stem cell-derived bipotential gonadal-like cells towards a steroidogenic cell fate

por Danti, Laura, Lundin, Karolina, Sepponen, Kirsi, Yohannes, Dawit A., Kere, Juha, Tuuri, Timo, Tapanainen, Juha S.
Publicado 2023