Association of LIN28B with adult adiposity-related traits in females. by Jaakko T Leinonen, Ida Surakka, Aki S Havulinna, Johannes Kettunen, Riitta Luoto, Veikko Salomaa, Elisabeth Widén

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Childhood adversities are associated with shorter telomere length at adult age both in individuals with an anxiety disorder and controls. by Laura Kananen, Ida Surakka, Sami Pirkola, Jaana Suvisaari, Jouko Lönnqvist, Leena Peltonen, Samuli Ripatti, Iiris Hovatta

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Genome-wide association studies reveal differences in genetic susceptibility between single events vs. recurrent events of atrial fibrillation and myocardial infarction: the HUNT s... by Martina Hall, Martina Hall, Anne Heidi Skogholt, Ida Surakka, Haavard Dalen, Haavard Dalen, Haavard Dalen, Eivind Almaas, Eivind Almaas

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ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. by Pyry Helkkula, Tuomo Kiiskinen, Aki S Havulinna, Juha Karjalainen, Seppo Koskinen, Veikko Salomaa, Mark J Daly, Aarno Palotie, Ida Surakka, Samuli Ripatti, FinnGen

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Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty. by Diana L Cousminer, Jaakko T Leinonen, Antti-Pekka Sarin, Himanshu Chheda, Ida Surakka, Karoliina Wehkalampi, Pekka Ellonen, Samuli Ripatti, Leo Dunkel, Aarno Palotie, Elisabeth Widén

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Mondo-Mlx Mediates Organismal Sugar Sensing through the Gli-Similar Transcription Factor Sugarbabe by Jaakko Mattila, Essi Havula, Erja Suominen, Mari Teesalu, Ida Surakka, Riikka Hynynen, Helena Kilpinen, Juho Väänänen, Iiris Hovatta, Reijo Käkelä, Samuli Ripatti, Thomas Sandmann, Ville Hietakangas

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Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals by Zewen Sun, Xingchen Pan, Aowen Tian, Ida Surakka, Tao Wang, Xu Jiao, Shanshan He, Jinfang Song, Xin Tian, Dan Tong, Jianping Wen, Yonggang Zhang, Wanqing Liu, Peng Chen

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Risk Factors for Early‐Onset Ischemic Stroke: A Case‐Control Study by Reetta Kivioja, Arto Pietilä, Nicolas Martinez‐Majander, Daniel Gordin, Aki S. Havulinna, Veikko Salomaa, Karoliina Aarnio, Sami Curtze, Jaana Leiviskä, Jorge Rodríguez‐Pardo, Ida Surakka, Markku Kaste, Turgut Tatlisumak, Jukka Putaala

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Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes. by Jussi Naukkarinen, Ida Surakka, Kirsi H Pietiläinen, Aila Rissanen, Veikko Salomaa, Samuli Ripatti, Hannele Yki-Järvinen, Cornelia M van Duijn, H-Erich Wichmann, Jaakko Kaprio, Marja-Riitta Taskinen, Leena Peltonen, ENGAGE Consortium

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Partial sleep restriction activates immune response-related gene expression pathways: experimental and epidemiological studies in humans. by Vilma Aho, Hanna M Ollila, Ville Rantanen, Erkki Kronholm, Ida Surakka, Wessel M A van Leeuwen, Maili Lehto, Sampsa Matikainen, Samuli Ripatti, Mikko Härmä, Mikael Sallinen, Veikko Salomaa, Matti Jauhiainen, Harri Alenius, Tiina Paunio, Tarja Porkka-Heiskanen

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The Contribution of GWAS Loci in Familial Dyslipidemias. by Pietari Ripatti, Joel T Rämö, Sanni Söderlund, Ida Surakka, Niina Matikainen, Matti Pirinen, Päivi Pajukanta, Antti-Pekka Sarin, Susan K Service, Pirkka-Pekka Laurila, Christian Ehnholm, Veikko Salomaa, Richard K Wilson, Aarno Palotie, Nelson B Freimer, Marja-Riitta Taskinen, Samuli Ripatti

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Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injury by Nicholas J. Douville, Nicholas J. Douville, Nicholas J. Douville, Daniel B. Larach, Adam Lewis, Lisa Bastarache, Anita Pandit, Jing He, Michael Heung, Michael Mathis, Michael Mathis, Michael Mathis, Jonathan P. Wanderer, Jonathan P. Wanderer, Sachin Kheterpal, Ida Surakka, Miklos D. Kertai

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A Novel Variant in APOB Gene Causes Extremely Low LDL-C Without Known Adverse Effects by Ida Surakka, PhD, Whitney E. Hornsby, PhD, Linda Farhat, MS, Melvyn Rubenfire, MD, Lars G. Fritsche, PhD, Kristian Hveem, MD, PhD, Y. Eugene Chen, MD, PhD, Robert D. Brook, MD, Cristen J. Willer, PhD, Richard L. Weinberg, MD, PhD

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The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits. by Josine L Min, Jennifer M Taylor, J Brent Richards, Tim Watts, Fredrik H Pettersson, John Broxholme, Kourosh R Ahmadi, Gabriela L Surdulescu, Ernesto Lowy, Christian Gieger, Chris Newton-Cheh, Markus Perola, Nicole Soranzo, Ida Surakka, Cecilia M Lindgren, Jiannis Ragoussis, Andrew P Morris, Lon R Cardon, Tim D Spector, Krina T Zondervan

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Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis by Sanni E. Ruotsalainen, Ida Surakka, Nina Mars, Juha Karjalainen, Mitja Kurki, Masahiro Kanai, Kristi Krebs, Sarah Graham, Pashupati P. Mishra, Binisha H. Mishra, Juha Sinisalo, Priit Palta, Terho Lehtimäki, Olli Raitakari, Estonian Biobank Research Team, Lili Milani, The Biobank Japan Project, Yukinori Okada, FinnGen, Aarno Palotie, Elisabeth Widen, Mark J. Daly, Samuli Ripatti

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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis by Sarah E. Graham, Jonas B. Nielsen, Matthew Zawistowski, Wei Zhou, Lars G. Fritsche, Maiken E. Gabrielsen, Anne Heidi Skogholt, Ida Surakka, Whitney E. Hornsby, Damian Fermin, Daniel B. Larach, Sachin Kheterpal, Chad M. Brummett, Seunggeun Lee, Hyun Min Kang, Goncalo R. Abecasis, Solfrid Romundstad, Stein Hallan, Matthew G. Sampson, Kristian Hveem, Cristen J. Willer

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Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2 by Yanbo Fan, Brooke N. Wolford, Haocheng Lu, Wenying Liang, Jinjian Sun, Wei Zhou, Oren Rom, Anubha Mahajan, Ida Surakka, Sarah E. Graham, Zhipeng Liu, Hyunbae Kim, Shweta Ramdas, Lars G. Fritsche, Jonas B. Nielsen, Maiken Elvestad Gabrielsen, Kristian Hveem, Dongshan Yang, Jun Song, Minerva T. Garcia-Barrio, Jifeng Zhang, Wanqing Liu, Kezhong Zhang, Cristen J. Willer, Y. Eugene Chen

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A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans by Marta R. Moksnes, Ailin F. Hansen, Brooke N. Wolford, Laurent F. Thomas, Humaira Rasheed, Anica Simić, Laxmi Bhatta, Anne Lise Brantsæter, Ida Surakka, Wei Zhou, Per Magnus, Pål R. Njølstad, Ole A. Andreassen, Tore Syversen, Jie Zheng, Lars G. Fritsche, David M. Evans, Nicole M. Warrington, Therese H. Nøst, Bjørn Olav Åsvold, Trond Peder Flaten, Cristen J. Willer, Kristian Hveem, Ben M. Brumpton

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MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk by Ida Surakka, Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu, Ben Brumpton, Jonas B. Nielsen, Maiken E. Gabrielsen, Anne Heidi Skogholt, Brooke Wolford, Sarah E. Graham, Y. Eugene Chen, Seunggeun Lee, Hyun Min Kang, Arnulf Langhammer, Siri Forsmo, Bjørn O. Åsvold, Unnur Styrkarsdottir, Hilma Holm, Daniel Gudbjartsson, Kari Stefansson, Aris Baras, Regeneron Genetics Center, Goncalo R. Abecasis, Kristian Hveem, Cristen J. Willer

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Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries by Seyedeh M. Zekavat, Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan Bloom, Timothy Poterba, Cotton Seed, Jason Ernst, Mark Chaffin, Jesse Engreitz, Gina M. Peloso, Ani Manichaikul, Chaojie Yang, Kathleen A. Ryan, Mao Fu, W. Craig Johnson, Michael Tsai, Matthew Budoff, Ramachandran S. Vasan, L. Adrienne Cupples, Jerome I. Rotter, Stephen S. Rich, Wendy Post, Braxton D. Mitchell, Adolfo Correa, Andres Metspalu, James G. Wilson, Veikko Salomaa, Manolis Kellis, Mark J. Daly, Benjamin M. Neale, Steven McCarroll, Ida Surakka, Tonu Esko, Andrea Ganna, Samuli Ripatti, Sekar Kathiresan, Pradeep Natarajan, NHLBI TOPMed Lipids Working Group

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