Expression of β-subunit of human chorionic gonadotropin genes during the normal and failed pregnancy

Por Rull, Kristiina, Laan, Maris
Publicado em 2005

The evolution and genomic landscape of CGB1 and CGB2 genes

Por Hallast, Pille, Rull, Kristiina, Laan, Maris
Publicado em 2007

Genetics of Recurrent Miscarriage: Challenges, Current Knowledge, Future Directions

Por Rull, Kristiina, Nagirnaja, Liina, Laan, Maris
Publicado em 2012

Methylation Allelic Polymorphism (MAP) in Chorionic Gonadotropin β5 (CGB5) and Its Association with Pregnancy Success

Por Uusküla, Liis, Rull, Kristiina, Nagirnaja, Liina, Laan, Maris
Publicado em 2011

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

Por Kasak, Laura, Rull, Kristiina, Sõber, Siim, Laan, Maris
Publicado no Sci Rep (2017)

Differential placental expression profile of human Growth Hormone/Chorionic Somatomammotropin genes in pregnancies with pre-eclampsia and gestational diabetes mellitus

Por Männik, Jaana, Vaas, Pille, Rull, Kristiina, Teesalu, Pille, Laan, Maris
Publicado em 2012

Extensive load of somatic CNVs in the human placenta

Por Kasak, Laura, Rull, Kristiina, Vaas, Pille, Teesalu, Pille, Laan, Maris
Publicado no Sci Rep (2015)

Differential Expression Profile of Growth Hormone/Chorionic Somatomammotropin Genes in Placenta of Small- and Large-for-Gestational-Age Newborns

Por Männik, Jaana, Vaas, Pille, Rull, Kristiina, Teesalu, Pille, Rebane, Tiina, Laan, Maris
Publicado em 2010

Genomics and genetics of gonadotropin beta-subunit genes: Unique FSHB and duplicated LHB/CGB loci

Por Nagirnaja, Liina, Rull, Kristiina, Uusküla, Liis, Hallast, Pille, Grigorova, Marina, Laan, Maris
Publicado em 2010

RNA sequencing of chorionic villi from recurrent pregnancy loss patients reveals impaired function of basic nuclear and cellular machinery

Por Sõber, Siim, Rull, Kristiina, Reiman, Mario, Ilisson, Piret, Mattila, Pirkko, Laan, Maris
Publicado no Sci Rep (2016)

A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage

Por Rull, Kristiina, Christiansen, Ole Bjarne, Nagirnaja, Liina, Steffensen, Rudi, Margus, Tõnu, Laan, Maris
Publicado em 2013

Annexin A5 Promoter Haplotype M2 Is Not a Risk Factor for Recurrent Pregnancy Loss in Northern Europe

Por Nagirnaja, Liina, Nõmmemees, Diana, Rull, Kristiina, Christiansen, Ole B., Nielsen, Henriette S., Laan, Maris
Publicado no PLoS One (2015)

Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators

Por Juhanson, Peeter, Rull, Kristiina, Kikas, Triin, Laivuori, Hannele, Vaas, Pille, Kajantie, Eero, Heinonen, Seppo, Laan, Maris
Publicado no J Clin Endocrinol Metab (2016)

Chorionic Gonadotropin Beta gene variants are associated with recurrent miscarriage in two European populations

Por Rull, Kristiina, Nagirnaja, Liina, Ulander, Veli-Matti, Kelgo, Piret, Margus, Tõnu, Kaare, Milja, Aittomäki, Kristiina, Laan, Maris
Publicado em 2008

Mid-Gestational Gene Expression Profile in Placenta and Link to Pregnancy Complications

Por Uusküla, Liis, Männik, Jaana, Rull, Kristiina, Minajeva, Ave, Kõks, Sulev, Vaas, Pille, Teesalu, Pille, Reimand, Jüri, Laan, Maris
Publicado em 2012

Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage

Por Nagirnaja, Liina, Palta, Priit, Kasak, Laura, Rull, Kristiina, Christiansen, Ole B, Nielsen, Henriette S, Steffensen, Rudi, Esko, Tõnu, Remm, Maido, Laan, Maris
Publicado no Hum Mutat (2014)

Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes

Por Sõber, Siim, Reiman, Mario, Kikas, Triin, Rull, Kristiina, Inno, Rain, Vaas, Pille, Teesalu, Pille, Marti, Jesus M. Lopez, Mattila, Pirkko, Laan, Maris
Publicado no Sci Rep (2015)

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

Por Nagirnaja, Liina, Venclovas, Česlovas, Rull, Kristiina, Jonas, Kim C., Peltoketo, Hellevi, Christiansen, Ole B., Kairys, Visvaldas, Kivi, Gaily, Steffensen, Rudi, Huhtaniemi, Ilpo T., Laan, Maris
Publicado em 2012

Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta

Por Metsalu, Tauno, Viltrop, Triin, Tiirats, Airi, Rajashekar, Balaji, Reimann, Ene, Kõks, Sulev, Rull, Kristiina, Milani, Lili, Acharya, Ganesh, Basnet, Purusotam, Vilo, Jaak, Mägi, Reedik, Metspalu, Andres, Peters, Maire, Haller-Kikkatalo, Kadri, Salumets, Andres
Publicado no Epigenetics (2014)