Mapping and identifying genes for asthma and psoriasis

Por Kere, Juha
Publicado em 2005

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

Por Katayama, Shintaro, Töhönen, Virpi, Linnarsson, Sten, Kere, Juha
Publicado em 2013

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

Por Wang, Jingwen, Vesterlund, Liselotte, Kere, Juha, Jiao, Hong
Publicado no PLoS One (2016)

A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene Region

Por Hannula, Katariina, Lipsanen-Nyman, Marita, Kontiokari, Tero, Kere, Juha
Publicado em 2001

Genetic evidence of multiple loci in dystocia - difficult labour

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

The zebrafish transcriptome during early development

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

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 em 2013

DCDC2 Polymorphism Is Associated with Left Temporoparietal Gray and White Matter Structures during Development

Por Darki, Fahimeh, Peyrard-Janvid, Myriam, Matsson, Hans, Kere, Juha, Klingberg, Torkel
Publicado no J Neurosci (2014)

Human ROBO1 Regulates Interaural Interaction in Auditory Pathways

Por Lamminmäki, Satu, Massinen, Satu, Nopola-Hemmi, Jaana, Kere, Juha, Hari, Riitta
Publicado no J Neurosci (2012)

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 no BMC Med Genet (2020)

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

Por Tapia-Páez, Isabel, Tammimies, Kristiina, Massinen, Satu, Roy, Ananda L., Kere, Juha
Publicado em 2008

A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18

Por Majander, Kerttu K, Villa, Pia M, Kivinen, Katja, Kere, Juha, Laivuori, Hannele
Publicado em 2013

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 no Sci Rep (2016)

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree of H19 Hypomethylation Associates with SRS Phenotype Severity and Genital and Skeletal Anomalies

Por Bruce, Sara, Hannula-Jouppi, Katariina, Peltonen, Jari, Kere, Juha, Lipsanen-Nyman, Marita
Publicado no Mol Endocrinol (2009)

Discovering heritable modes of MEG spectral power

Por Leppäaho, Eemeli, Renvall, Hanna, Salmela, Elina, Kere, Juha, Salmelin, Riitta, Kaski, Samuel
Publicado no Hum Brain Mapp (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 no BMC Bioinformatics (2019)

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 em 2012-02-01

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 em 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 em 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 no BMJ Open (2016)