Publications (1061)

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Gender diversity and firm value: Evidence from UK financial institutions
(2019)
International Journal of Accounting and Information Management
Peter Agyemang-Mintah, Hannu Schadewitz
Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families
(2019)
Diabetes
Hippich M, Beyerlein A, Hagopian WA, Krischer JP, Vehik K, Knoop J, Winker C, Toppari J, Lernmark A, Rewers MJ, Steck AK, She JX, Akolkar B, Robertson CC, Onengut-Gumuscu S, Rich SS, Bonifacio E, Ziegler AG
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
(2019)
Nature Genetics
Sakornsakolpat P, Prokopenko D, Lamontagne M, Reeve NF, Guyatt AL, Jackson VE, Shrine N, Qiao DD, Bartz TM, Kim DK, Lee MK, Latourelle JC, Li XN, Morrow JD, Obeidat M, Wyss AB, Bakke P, Barr RG, Beaty TH, Belinsky SA, Brusselle GG, Crapo JD, de Jong K, DeMeo DL, Fingerlin TE, Gharib SA, Gulsvik A, Hall IP, Hokanson JE, Kim WJ, Lomas DA, London SJ, Meyers DA, O'Connor GT, Rennard SI, Schwartz DA, Sliwinski P, Sparrow D, Strachan DP, Tal-Singer R, Tesfaigzi Y, Vestbo J, Vonk JM, Yim JJ, Zhou XB, Bosse Y, Manichaikul A, Lahousse L, Silverman EK, Boezen HM, Wain LV, Tobin MD, Hobbs BD, Cho; SpiroMeta Consortium & International COPD Genetics Consortium
Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008
(2019)
British Journal of Haematology
Sofie G. Højfeldt, Benjamin O. Wolthers, Morten Tulstrup, Jonas Abrahamsson, Ramneek Gupta, Arja Harila-Saari, Mats Heyman, Louise T. Henriksen, Òlafur G. Jónsson, Päivi M. Lähteenmäki, Bendik Lund, Kaie Pruunsild, Goda Vaitkeviciene, Kjeld Schmiegelow, Birgitte K. Albertsen; on behalf of the Nordic Society of Paediatric Haematology Oncology (NOPHO) group
Genetic risk factors for schizophrenia associate with sleep spindle activity in healthy adolescents
(2019)
Journal of Sleep Research
Merikanto I, Utge S, Lahti J, Kuula L, Makkonen T, Lahti-Pulkkinen M, Heinonen K, Raikkonen K, Andersson S, Strandberg T, Pesonen AK
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
(2019)
Nature Genetics
Linner RK, Biroli P, Kong E, Meddens FW, Wedow R, Fontana MA, Lebreton M, Tino SP, Abdellaoui A, Hammerschlag AR, Nivard MG, Okbay A, Rietveld CA, Timshel PN, Trzaskowski M, Vlaming R, Zund CL, Bao YC, Buzdugan L, Caplin AH, Chen CY, Eibich P, Fontanillas P, Gonzalez JR, Joshi PK, Karhunen V, Kleinman A, Levin RZ, Lill CM, Meddens GA, Muntane G, Sanchez-Roige S, Rooij FJ, Taskesen E, Wu Y, Zhang FT, Agee M, Alipanahi B, Bell RK, Bryc K, Elson SL, Furlotte NA, Huber KE, Litterman NK, McCreight JC, McIntyre MH, Mountain JL, Northover CAM, Pitts SJ, Sathirapongsasuti JF, Sazonova OV, Shelton JF, Shringarpure S, Tian C, Tung JY, Vacic V, Wilson CH, Agbessi M, Ahsan H, Alves I, Andiappan A, Awadalla P, Battle A, Beutner F, Bonder MJ, Boomsma DI, Christiansen M, Claringbould A, Deelen P, Esko T, Fave MJ, Franke L, Frayling T, Gharib SA, Gibson G, Heijmans B, Hemani G, Jansen R, Kahonen M, Kalnapenkis A, Kasela S, Kettunen J, Kim Y, Kirsten H, Kovacs P, Krohn K, Kronberg-Guzman J, Kukushkina V, Kutalik Z, Lee B, Lehtimaki T, Loeffler M, Marigorta UM, Metspalu A, Milani L, Montgomery GW, Mueller-Nurasyid M, Nauck M, Penninx B, Perola M, Pervjakova N, Pierce B, Powell J, Prokisch H, Psaty BM, Raitakari O, Ring S, Ripatti S, Rotzchke O, Rueger S, Saha A, Scholz M, Schramm K, Seppala I, Stumvoll M, Sullivan P, Hoen PB, Teumer A, Thiery J, Tong L, Tonjes A, van Dongen J, van Meurs J, Verlouw J, Visscher PM, Volker U, Vosa U, Westra HJ, Yaghootkar H, Yang J, Zeng B, Lee JJ, Pers TH, Turley P, Chen GB, Emilsson V, Oskarsson S, Pickrell JK, Thom K, Timshel P, Ahluwalia TS, Bacelis J, Baumbach C, Bjornsdottir G, Brandsma JH, Concas MP, Derringer J, Furlotte NA, Galesloot TE, Girotto G, Gupta R, Hall LM, Harris SE, Hofer E, Horikoshi M, Huffman JE, Kaasik K, Kalafati IP, Kong A, Lahti J, Lee SJD, Leeuw C, Lind PA, Lindgren KO, Liu T, Mangino M, Marten J, Mihailov E, Miller MB, Most PJD, Oldmeadow C, Payton A, Pervjakova N, Peyrot WJ, Qian Y, Raitakari O, Rueedi R, Salvi E, Schmidt B, Schraut KE, Shi J, Smith AV, Poot RA, Pourcain B, Teumer A, Thorleifsson G, Verweij N, Vuckovic D, Wellmann J, Westra HJ, Yang JY, Zhao W, Zhu ZH, Alizadeh BZ, Amin N, Bakshi A, Baumeister SE, Biino G, Bonnelykke K, Boyle PA, Campbell H, Cappuccio FP, Davies G, De Neve JE, Deloukas P, Demuth I, Ding J, Eibich P, Eisele L, Eklund N, Evans DM, Faul JD, Feitosa MF, Forstner AJ, Gandin I, Gunnarsson B, Halldorsson BV, Harris TB, Heath AC, Hocking LJ, Holliday EG, Homuth G, Horan MA, Hottenga JJ, Jager PL, Jugessur A, Kaakinen MA, Kahonen M, Kanoni S, Keltigangas-Jarvinen L, Kiemeney LALM, Kolcic I, Koskinen S, Kraja AT, Kroh M, Kutalik Z, Latvala A, Launer LJ, Lebreton MP, Levinson DF, Lichtenstein P, Lichtner P, Liewald DCM, Loukola A, Madden PA, Magi R, Maki-Opas T, Marioni RE, Marques-Vidal P, McMahon G, Meisinger C, Meitinger T, Milaneschi Y, Milani L, Montgomery GW, Myhre R, Nelson CP, Nyholt DR, Ollier WER, Palotie A, Paternoster L, Pedersen NL, Petrovic KE, Porteous DJ, Raikkonen K, Ring SM, Robino A, Rostapshova O, Rudan I, Rustichini A, Salomaa V, Sanders AR, Sarin AP, Schmidt H, Scott RJ, Smith BH, Smith JA, Staessen JA, Steinhagen-Thiessen E, Strauch K, Terracciano A, Tobin MD, Ulivi S, Vaccargiu S, Quaye L, Venturini C, Vinkhuyzen AAE, Volker U, Voelzke H, Vonk JM, Vozzi D, Waage J, Ware EB, Willemsen G, Attia JR, Bennett DA, Berger K, Bertram L, Bisgaard H, Boomsma DI, Borecki IB, Bultmann U, Chabris CF, Cucca F, Cusi D, Deary J, Dedoussis GV, Duijn CM, Eriksson JG, Franke B, Franke L, Gasparini P, Gejman PV, Gieger C, Grabe HJ, Gratten J, Gudnason V, Harst PD, Hayward C, Hinds DA, Hoffmann W, Hypponen E, Iacono WG, Jacobsson B, Jarvelin MR, Jockel KH, Kaprio J, Kardia SLR, Lehtimaki T, Lehrer SF, Magnusson PKE, Martin NG, Mcgue M, Metspalu A, Pendleton N, Penninx B, Perola M, Pirastu N, Pirastu M, Polasek O, Posthuma D, Power C, Province MA, Samani NJ, Schlessinger D, Schmidt R, Sorensen TIA, Spector TD, Stefansson K, Thorsteinsdottir U, Thurik AR, Timpson NJ, Tiemeier H, Tung JY, Uitterlinden AG, Vitart V, Vollenweider P, Weir DR, Wilson JF, Wright AF, Conley DC, Krueger RF, Smith GD, Laibson DI, Medland SE, Yang J, Johannesson M, Visscher PM, Esko T, Koellinger PD, Cesarini D, Benjamin DJ, Auton A, Boardman JD, Clark DW, Conlin A, Dolan CC, Fischbacher U, Groenen PJF, Harris KM, Hasler G, Hofman A, Ikram MA, Jain S, Karlsson R, Kessler RC, Kooyman M, MacKillop J, Mannikko M, Morcillo-Suarez C, McQueen MB, Schmidt KM, Smart MC, Sutter M, Thurik AR, Uitterlinden AG, White J, de Wit H, Yang J, Bertram L, Boomsma DI, Esko T, Fehr E, Hinds DA, Johannesson M, Kumari M, Laibson D, Magnusson PKE, Meyer MN, Navarro A, Palmer AA, Pers TH, Posthuma D, Schunk D, Stein MB, Svento R, Tiemeier H, Timmers PRHJ, Turley P, Ursano RJ, Wagner GG, Wilson JF, Gratten J, Lee JJ, Cesarini D, Benjamin DJ, Koellinger PD, Beauchamp JP, Cesarini D, Lee JJ, Koellinger PD, Benjamin DJ, Beauchamp JP, Gratten J
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
(2019)
European Journal of Human Genetics
Hottenga J., Iorio A., Kors J., Linneberg A., Ford I., Hansen T., Harris T., Heckbert S., Silva Aldana C., Sinagra G., Sinner M., Soliman E., MacFarlane P., Meitinger T., Nelson C., Raitakari O., Gasparini P., Alonso A., Jamshidi Y., Gudnason V., Uitterlinden A., Stoll M., Waldenberger M., van Duijn C., Samani N., Peters A., Ulivi S., Sotoodehnia N., Kanters J., Kääb S., Munroe P., Lehtimäki T., Isaacs A., van der Harst P., de Bakker P., Jukema J., Stricker B., Wilson J., de Geus E., van Setten J., Verweij N., Trompet S., Arking D., Mbarek H., Niemeijer M., Hall L., Grarup N., Gandin I., Brody J., Müller-Nurasyid M., Mei H., Lyytikäinen L., Hemerich D., Warren H., Smith A., Robino A., Prins B., Eijgelsheim M., Caulfield M., Boomsma D., Asselbergs F.
Genome-wide CRISPR Screens in T Helper Cells Reveal Pervasive Crosstalk between Activation and Differentiation
(2019)
Cell
Henriksson J, Chen X, Gomes T, Ullah U, Meyer KB, Miragaia R, Duddy G, Pramanik J, Yusa K, Lahesmaa R, Teichmann SA
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