Results 201 to 210 of about 6,310 (247)

Causal and shared genetic insights into severe COVID-19 and idiopathic pulmonary fibrosis. [PDF]

iScience
Lin S, Dang X, Kou X, Zhang X, Ding X, Li X.   +5 more
europepmc   +1 more source

ADH7 and plasma proteins mediate smoking-related esophageal cancer: genetic causality and therapeutic insight. [PDF]

Front Med (Lausanne)
Pan L, Yang X, Hao Q, Xie K, Ma H.
europepmc   +1 more source

OmicsPred as a centralised resource for genetic prediction of multi-omic traits

Foguet C, Gil L, Xu Y, Salazar-Magaña S, Ritchie SC, Persyn E, Im HK, Inouye M, Lambert SA.   +8 more
europepmc   +1 more source

Privacy-enhancing sequential learning under heterogeneous selection bias in multi-site electronic health records data. [PDF]

J Am Med Inform Assoc
Kundu R, Salvatore M, Patel KK, Ohno-Machado L, Cho H, Shi X, Mukherjee B.   +6 more
europepmc   +1 more source

Phenome-wide association of multiallelic copy number variation in 422,170 UK Biobank individuals reveals novel genetic loci associated with disease

Eisenberg M, Packer R, Shrine N, Demidov G, Pack H, Hollox EJ, Fawcett K.   +6 more
europepmc   +1 more source

Genetic determinants of childhood blood pressure and heart rate in relation to adult health outcomes: the consortium of childhood blood pressure. [PDF]

Eur Heart J
Xie T, Ani A, Vaez A, Nolte IM, Su S, Ishikuro M, Wang S, Zhang W, Soares AG, Motazedi E, Calas L, Ronkainen J, Pedersen CT, Lu X, Stinson SE, Felix JF, Stankevic E, Wang CA, Thiering E, Fernández D, Calvo-Serra B, Stathopoulou MG, Fore R, Kumar A, Tuhkanen J, Bilbao JR, Ibarluzea J, Isaacs A, Fonvig CE, Rivadeneira F, Lund MAV, Holm LA, van der Most PJ, Riese H, Narita A, Tamiya G, Flexeder C, Wiersma R, Argoty-Pantoja AD, Vinding R, Hansen TW, Kümler T, Estarlich M, Bustamante M, Yuan WL, Boland-Augé A, Deleuze JF, Petrelis AM, Rifas-Shiman S, Kajantie E, Fernandez-Jimenez N, Santa-Marina L, Arts ICW, Lahti J, Strandberg T, Kull I, Bergström A, Hivert MF, Bønnelykke K, Kuriyama S, Beilin LJ, Mori TA, Hartman CA, Grarup N, Thijs C, Räikkönen K, Melén E, Oken E, Visvikis-Siest S, Gützkow KB, Grazuleviciene R, Heude B, Chatzi L, Vrijheid M, Standl M, Vrijkotte T, Pennell CE, Oldehinkel AJ, Hansen T, Jaddoe VWV, Holm JC, Sebert S, Timpson NJ, Obara T, Wang X, Lawlor DA, Corpeleijn E, Ahluwalia TS, Snieder H, Lifelines Cohort Study, ICBP Consortium.   +90 more
europepmc   +1 more source

Genetic architecture of a Circadian Imbalance Index: genome-wide association, phenome-wide association, and Mendelian randomisation analyses. [PDF]

EBioMedicine
Żebrowska M, Wielscher M, Zhang J, Saksvik-Lehouillier I, DiMilia L, Burns A, Valliere J, Vincenzi L, Redline S, Okereke O, Saxena R, Richmond R, Rutter MK, Schernhammer ES.   +13 more
europepmc   +1 more source

Causal associations between plasma proteins and premature ovarian failure through multi-omics Mendelian randomization analyses. [PDF]

Gynecol Pelvic Med
Wang C, Cheng M.
europepmc   +1 more source

Comment on "Discovery of Potential New Drug Targets for Osteoporosis of Various Subtypes With or Without Pathological Fracture Complications: A Drug Target Mendelian Randomization Study". [PDF]

Geriatr Gerontol Int
Zhao Z, Shen T.
europepmc   +1 more source

Integrating multi-omics and mendelian randomization identifies therapeutic targets for Lichen Sclerosus: A druggable genome-wide study. [PDF]

Glob Med Genet
Wang S, Wang P, Li H, Guan X, Ji S, Zhang X, Chen Y, Li N, Li H, Xue L, Zhao C.   +10 more
europepmc   +1 more source