Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 37 Records) |
Query Trace: PAPPA[original query] |
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Association of the RANTES gene promoter polymorphisms -28C/G and -403G/A with pneumonia in Greek children. International journal of immunopathology and pharmacology 0 26 (3): 681-90. Doudouliaki T, Haidopoulou K, Pappa S, Sakellaropoulou A, Tsakiridis P, Emboriadou M, Hatzistilianou |
A study of ERa PvuII polymorphism in female patients with acute stroke: no associations with disease severity and early outcome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2013 Aug 29 (8): 784-7. Pappa Theodora, Vemmos Konstantinos, Stamatelopoulos Kimon, Mantzou Emily, Georgiopoulos George, Markoula Sofia, Zakopoulos Nikolaos, Alevizaki Mar |
DRD4 VNTRs, observed stranger fear in preschoolers and later ADHD symptoms. Psychiatry research 2014 Dec 220 (3): 982-6. Pappa Irene, Mileva-Seitz Viara R, Szekely Eszter, Verhulst Frank C, Bakermans-Kranenburg Marian J, Jaddoe Vincent W V, Hofman Albert, Tiemeier Henning, van IJzendoorn Marinus |
A genome-wide association meta-analysis of preschool internalizing problems.
Journal of the American Academy of Child and Adolescent Psychiatry 2014 Jun 53 (6): 667-676.e7. Benke Kelly S, Nivard Michel G, Velders Fleur P, Walters Raymond K, Pappa Irene, Scheet Paul A, Xiao Xiangjun, Ehli Erik A, Palmer Lyle J, Whitehouse Andrew J O, Verhulst Frank C, Jaddoe Vincent W, Rivadeneira Fernando, Groen-Blokhuis Maria M, van Beijsterveldt Catharina E M, Davies Gareth E, Hudziak James J, Lubke Gitta H, Boomsma Dorret I, Pennell Craig E, Tiemeier Henning, Middeldorp Christel M, |
Single Nucleotide Polymorphism Heritability of Behavior Problems in Childhood: Genome-Wide Complex Trait Analysis. Journal of the American Academy of Child and Adolescent Psychiatry 2015 Sep 54 (9): 737-44. Pappa Irene, Fedko Iryna O, Mileva-Seitz Viara R, Hottenga Jouke-Jan, Bakermans-Kranenburg Marian J, Bartels Meike, van Beijsterveldt Catharina E M, Jaddoe Vincent W V, Middeldorp Christel M, Rippe Ralph C A, Rivadeneira Fernando, Tiemeier Henning, Verhulst Frank C, van IJzendoorn Marinus H, Boomsma Dorret |
The magnificent seven: A quantitative review of dopamine receptor d4 and its association with child behavior. Neuroscience and biobehavioral reviews 2015 Aug 57 175-186. Pappa Irene, Mileva-Seitz Viara R, Bakermans-Kranenburg Marian J, Tiemeier Henning, van IJzendoorn Marinus |
Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height. Behavior genetics 2015 Sep 45 (5): 514-28. Fedko Iryna O, Hottenga Jouke-Jan, Medina-Gomez Carolina, Pappa Irene, van Beijsterveldt Catharina E M, Ehli Erik A, Davies Gareth E, Rivadeneira Fernando, Tiemeier Henning, Swertz Morris A, Middeldorp Christel M, Bartels Meike, Boomsma Dorret |
A genome-wide approach to children's aggressive behavior: The EAGLE consortium.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 Jul 171 (5): 562-72. Pappa Irene, St Pourcain Beate, Benke Kelly, Cavadino Alana, Hakulinen Christian, Nivard Michel G, Nolte Ilja M, Tiesler Carla M T, Bakermans-Kranenburg Marian J, Davies Gareth E, Evans David M, Geoffroy Marie-Claude, Grallert Harald, Groen-Blokhuis Maria M, Hudziak James J, Kemp John P, Keltikangas-Järvinen Liisa, McMahon George, Mileva-Seitz Viara R, Motazedi Ehsan, Power Christine, Raitakari Olli T, Ring Susan M, Rivadeneira Fernando, Rodriguez Alina, Scheet Paul A, Seppälä Ilkka, Snieder Harold, Standl Marie, Thiering Elisabeth, Timpson Nicholas J, Veenstra René, Velders Fleur P, Whitehouse Andrew J O, Smith George Davey, Heinrich Joachim, Hypponen Elina, Lehtimäki Terho, Middeldorp Christel M, Oldehinkel Albertine J, Pennell Craig E, Boomsma Dorret I, Tiemeier Henni |
Beyond the usual suspects: a multidimensional genetic exploration of infant attachment disorganization and security. Attachment & human development 2015 17 (3): 288-301. Pappa Irene, Szekely Eszter, Mileva-Seitz Viara R, Luijk Maartje P C M, Bakermans-Kranenburg Marian J, van IJzendoorn Marinus H, Tiemeier Henni |
Elevated P3b latency variability in carriers of ZNF804A risk allele for psychosis. NeuroImage 2015 Aug 116 207-13. Saville Christopher W N, Lancaster Thomas M, Davies Timothy J, Toumaian Maida, Pappa Eleni, Fish Simon, Feige Bernd, Bender Stephan, Mantripragada Kiran K, Linden David E J, Klein Christo |
Genetic screening of patients with medullary thyroid cancer in a referral center in Greece during the past two decades. European journal of endocrinology / European Federation of Endocrine Societies 2015 Apr 172 (4): 501-9. Sarika H-L, Papathoma A, Garofalaki M, Saltiki K, Pappa T, Pazaitou-Panayiotou K, Anastasiou E, Alevizaki |
The role of TLR4 and CD14 polymorphisms in the pathogenesis of respiratory syncytial virus bronchiolitis in greek infants. International journal of immunopathology and pharmacology 0 27 (4): 563-72. Goutaki M, Haidopoulou K, Pappa S, Tsakiridis P, Frydas E, Eboriadou M, Hatzistylianou |
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.
Journal of the American Academy of Child and Adolescent Psychiatry 2016 Oct 55 (10): 896-905.e6. Middeldorp Christel M, Hammerschlag Anke R, Ouwens Klaasjan G, Groen-Blokhuis Maria M, St Pourcain Beate, Greven Corina U, Pappa Irene, Tiesler Carla M T, Ang Wei, Nolte Ilja M, Vilor-Tejedor Natalia, Bacelis Jonas, Ebejer Jane L, Zhao Huiying, Davies Gareth E, Ehli Erik A, Evans David M, Fedko Iryna O, Guxens Mònica, Hottenga Jouke-Jan, Hudziak James J, Jugessur Astanand, Kemp John P, Krapohl Eva, Martin Nicholas G, Murcia Mario, Myhre Ronny, Ormel Johan, Ring Susan M, Standl Marie, Stergiakouli Evie, Stoltenberg Camilla, Thiering Elisabeth, Timpson Nicholas J, Trzaskowski Maciej, van der Most Peter J, Wang Carol, , Nyholt Dale R, Medland Sarah E, Neale Benjamin, Jacobsson Bo, Sunyer Jordi, Hartman Catharina A, Whitehouse Andrew J O, Pennell Craig E, Heinrich Joachim, Plomin Robert, Davey Smith George, Tiemeier Henning, Posthuma Danielle, Boomsma Dorret |
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium. Sleep 2016 Oct 39 (10): 1859-1869. Marinelli Marcella, Pappa Irene, Bustamante Mariona, Bonilla Carolina, Suarez Anna, Tiesler Carla M, Vilor-Tejedor Natalia, Zafarmand Mohammad Hadi, Alvarez-Pedrerol Mar, Andersson Sture, Bakermans-Kranenburg Marian J, Estivill Xavier, Evans David M, Flexeder Claudia, Forns Joan, Gonzalez Juan R, Guxens Monica, Huss Anke, van IJzendoorn Marinus H, Jaddoe Vincent W V, Julvez Jordi, Lahti Jari, López-Vicente Mónica, Lopez-Espinosa Maria-Jose, Manz Judith, Mileva-Seitz Viara R, Perola Markus, Pesonen Anu-Katriina, Rivadeneira Fernando, Salo Perttu P, Shahand Shayan, Schulz Holger, Standl Marie, Thiering Elisabeth, Timpson Nicholas J, Torrent Maties, Uitterlinden André G, Smith George Davey, Estarlich Marisa, Heinrich Joachim, Räikkönen Katri, Vrijkotte Tanja G M, Tiemeier Henning, Sunyer Jor |
Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence. PloS one 2016 11 (6): e0157739. Cáceres Alejandro, Esko Tõnu, Pappa Irene, Gutiérrez Armand, Lopez-Espinosa Maria-Jose, Llop Sabrina, Bustamante Mariona, Tiemeier Henning, Metspalu Andres, Joshi Peter K, Wilsonx James F, Reina-Castillón Judith, Shin Jean, Pausova Zdenka, Paus Tomáš, Sunyer Jordi, Pérez-Jurado Luis A, González Juan |
FKBP5 interacts with maltreatment in children with extreme, pervasive, and persistent aggression. Psychiatry research 2016 Aug 242 277-80. Bryushkova Lyubov, Zai Clement, Chen Sheng, Pappa Irene, Mileva Viara, Tiemeier Henning, Bakermans-Kranenburg Marian, Kennedy James L, Beitchman Joseph |
Single Nucleotide Polymorphism Heritability of a General Psychopathology Factor in Children. Journal of the American Academy of Child and Adolescent Psychiatry 2016 Dec 55 (12): 1038-1045.e4. Neumann Alexander, Pappa Irene, Lahey Benjamin B, Verhulst Frank C, Medina-Gomez Carolina, Jaddoe Vincent W, Bakermans-Kranenburg Marian J, Moffitt Terrie E, van IJzendoorn Marinus H, Tiemeier Henni |
Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population. European journal of human genetics : EJHG 2017 May . Vojinovic Dina, Brison Nathalie, Ahmad Shahzad, Noens Ilse, Pappa Irene, Karssen Lennart C, Tiemeier Henning, van Duijn Cornelia M, Peeters Hilde, Amin Naj |
The Q192R polymorphism of the paraoxonase-1 (PON1) gene is associated with susceptibility to gestational diabetes mellitus in the Greek population. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2017 Mar 1-4. Pappa Kalliopi I, Gazouli Maria, Anastasiou Eleni, Loutradis Dimitrios, Anagnou Nicholas |
Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior. JAMA psychiatry 2017 Oct . Tielbeek Jorim J, Johansson Ada, Polderman Tinca J C, Rautiainen Marja-Riitta, Jansen Philip, Taylor Michelle, Tong Xiaoran, Lu Qing, Burt Alexandra S, Tiemeier Henning, Viding Essi, Plomin Robert, Martin Nicholas G, Heath Andrew C, Madden Pamela A F, Montgomery Grant, Beaver Kevin M, Waldman Irwin, Gelernter Joel, Kranzler Henry R, Farrer Lindsay A, Perry John R B, Munafò Marcus, LoParo Devon, Paunio Tiina, Tiihonen Jari, Mous Sabine E, Pappa Irene, de Leeuw Christiaan, Watanabe Kyoko, Hammerschlag Anke R, Salvatore Jessica E, Aliev Fazil, Bigdeli Tim B, Dick Danielle, Faraone Stephen V, Popma Arne, Medland Sarah E, Posthuma Danielle, |
The genetic component of human longevity: New insights from the analysis of pathway-based SNP-SNP interactions. Aging cell 2018 Mar e12755. Dato Serena, Soerensen Mette, De Rango Francesco, Rose Giuseppina, Christensen Kaare, Christiansen Lene, Passarino Giusep |
ASXL1 mutations in AML are associated with specific clinical and cytogenetic characteristics. Leukemia & lymphoma 2018 Feb 1-8. Kakosaiou Katerina, Panitsas Fotios, Daraki Aggeliki, Pagoni Maria, Apostolou Paraskevi, Ioannidou Agapi, Vlachadami Ioanna, Marinakis Theodoros, Giatra Chara, Vasilatou Diamantina, Sambani Constantina, Pappa Vassiliki, Manola Kalliopi |
Myelodysplastic syndromes and idiopathic pulmonary fibrosis: a dangerous liaison. Respiratory research 2019 8 20 (1): 182. Papiris Spyros A, Tsirigotis Panagiotis, Kannengiesser Caroline, Kolilekas Lykourgos, Gkirkas Konstantinos, Papaioannou Andriana I, Revy Patrick, Giouleka Paschalina, Papadaki Georgia, Kagouridis Konstantinos, Pappa Vassiliki, Borie Raphael, Boileau Catherine, Bouros Demosthenes, Crestani Bruno, Manali Effrosyni |
The Genetic Variations Associated With Time to Aseptic Loosening After Total Joint Arthroplasty.
The Journal of arthroplasty 2020 Apr 35 (4): 981-988. Koks Sulev, Wood David J, Reimann Ene, Awiszus Friedemann, Lohmann Christoph H, Bertrand Jessica, Prans Ele, Maasalu Katre, Märtson Aa |
Author Correction: A common variant of the pregnancy-associated plasma protein-A (PAPPA) gene encodes a protein with reduced proteolytic activity towards IGF-binding proteins. Scientific reports 2019 11 9 (1): 17523. Bøtkjær J A, Noer P R, Oxvig Claus, Andersen Claus Ydi |
Does height and IGF-I determine pubertal timing in girls? Pediatric research 2020 11 90 (1): 176-183. Upners Emmie N, Busch Alexander S, Almstrup Kristian, Petersen Jørgen H, Assens Maria, Main Katharina M, Jensen Rikke B, Juul Ande |
Identification and characterization of a rare variant in apolipoprotein A-IV, p.(V336M), and evaluation of HDL functionality in a Greek cohort with extreme HDL cholesterol levels. Archives of biochemistry and biophysics 2020 11 696 108655. Chroni Angeliki, Rallidis Loukianos, Vassou Despoina, Gkolfinopoulou Christina, Papakosta Paraskevi, Zervou Maria I, Goulielmos George N, Kiouri Estela, Pappa Danae, Eliopoulos Elias, Kardassis Dimitr |
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Nature metabolism 2020 10 2 (10): 1135-1148. Folkersen Lasse, Gustafsson Stefan, Wang Qin, Hansen Daniel Hvidberg, Hedman Åsa K, Schork Andrew, Page Karen, Zhernakova Daria V, Wu Yang, Peters James, Eriksson Niclas, Bergen Sarah E, Boutin Thibaud S, Bretherick Andrew D, Enroth Stefan, Kalnapenkis Anette, Gådin Jesper R, Suur Bianca E, Chen Yan, Matic Ljubica, Gale Jeremy D, Lee Julie, Zhang Weidong, Quazi Amira, Ala-Korpela Mika, Choi Seung Hoan, Claringbould Annique, Danesh John, Davey Smith George, de Masi Federico, Elmståhl Sölve, Engström Gunnar, Fauman Eric, Fernandez Celine, Franke Lude, Franks Paul W, Giedraitis Vilmantas, Haley Chris, Hamsten Anders, Ingason Andres, Johansson Åsa, Joshi Peter K, Lind Lars, Lindgren Cecilia M, Lubitz Steven, Palmer Tom, Macdonald-Dunlop Erin, Magnusson Martin, Melander Olle, Michaelsson Karl, Morris Andrew P, Mägi Reedik, Nagle Michael W, Nilsson Peter M, Nilsson Jan, Orho-Melander Marju, Polasek Ozren, Prins Bram, Pålsson Erik, Qi Ting, Sjögren Marketa, Sundström Johan, Surendran Praveen, Võsa Urmo, Werge Thomas, Wernersson Rasmus, Westra Harm-Jan, Yang Jian, Zhernakova Alexandra, Ärnlöv Johan, Fu Jingyuan, Smith J Gustav, Esko Tõnu, Hayward Caroline, Gyllensten Ulf, Landen Mikael, Siegbahn Agneta, Wilson James F, Wallentin Lars, Butterworth Adam S, Holmes Michael V, Ingelsson Erik, Mälarstig Ande |
Pharmacogenetic analysis of canonical versus noncanonical pathway of NF-kB in Crohn's disease patients under anti-tumor necrosis factor-? treatment. Pharmacogenetics and genomics 2022 Aug 32 (6): 235-241. Stavrou Eleana F, Chatzopoulou Fani, Antonatos Charalabos, Pappa Panagiota, Makridou Eutychia, Oikonomou Konstantinos, Kapsoritakis Andreas, Potamianos Petros S, Karmiris Konstantinos, Tzathas Charalambos, Chatzidimitriou Dimitris, Vizirianakis Ioannis S, Vasilopoulos Yiann |
Deregulated DNA damage response network in Behcet's disease. Clinical immunology (Orlando, Fla.) 2022 11 246 109189. Vlachogiannis Nikolaos I, Ntouros Panagiotis A, Pappa Maria, Verrou Kleio-Maria, Arida Aikaterini, Souliotis Vassilis L, Sfikakis Petros |
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- Page last updated:Jun 11, 2024
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