Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 293 Records) |
Query Trace: INA[original query] |
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Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.
Acta neuropathologica 2022 Sep . Jansen Iris E, van der Lee Sven J, Gomez-Fonseca Duber, de Rojas Itziar, Dalmasso Maria Carolina, Grenier-Boley Benjamin, Zettergren Anna, Mishra Aniket, Ali Muhammad, Andrade Victor, Bellenguez Céline, Kleineidam Luca, Küçükali Fahri, Sung Yun Ju, Tesí Niccolo, Vromen Ellen M, Wightman Douglas P, Alcolea Daniel, Alegret Montserrat, Alvarez Ignacio, Amouyel Philippe, Athanasiu Lavinia, Bahrami Shahram, Bailly Henri, Belbin Olivia, Bergh Sverre, Bertram Lars, Biessels Geert Jan, Blennow Kaj, Blesa Rafael, Boada Mercè, Boland Anne, Buerger Katharina, Carracedo Ángel, Cervera-Carles Laura, Chene Geneviève, Claassen Jurgen A H R, Debette Stephanie, Deleuze Jean-Francois, de Deyn Peter Paul, Diehl-Schmid Janine, Djurovic Srdjan, Dols-Icardo Oriol, Dufouil Carole, Duron Emmanuelle, Düzel Emrah, , Fladby Tormod, Fortea Juan, Frölich Lutz, García-González Pablo, Garcia-Martinez Maria, Giegling Ina, Goldhardt Oliver, Gobom Johan, Grimmer Timo, Haapasalo Annakaisa, Hampel Harald, Hanon Olivier, Hausner Lucrezia, Heilmann-Heimbach Stefanie, Helisalmi Seppo, Heneka Michael T, Hernández Isabel, Herukka Sanna-Kaisa, Holstege Henne, Jarholm Jonas, Kern Silke, Knapskog Anne-Brita, Koivisto Anne M, Kornhuber Johannes, Kuulasmaa Teemu, Lage Carmen, Laske Christoph, Leinonen Ville, Lewczuk Piotr, Lleó Alberto, de Munain Adolfo López, Lopez-Garcia Sara, Maier Wolfgang, Marquié Marta, Mol Merel O, Montrreal Laura, Moreno Fermin, Moreno-Grau Sonia, Nicolas Gael, Nöthen Markus M, Orellana Adelina, Pålhaugen Lene, Papma Janne M, Pasquier Florence, Perneczky Robert, Peters Oliver, Pijnenburg Yolande A L, Popp Julius, Posthuma Danielle, Pozueta Ana, Priller Josef, Puerta Raquel, Quintela Inés, Ramakers Inez, Rodriguez-Rodriguez Eloy, Rujescu Dan, Saltvedt Ingvild, Sanchez-Juan Pascual, Scheltens Philip, Scherbaum Norbert, Schmid Matthias, Schneider Anja, Selbæk Geir, Selnes Per, Shadrin Alexey, Skoog Ingmar, Soininen Hilkka, Tárraga Lluís, Teipel Stefan, , Tijms Betty, Tsolaki Magda, Van Broeckhoven Christine, Van Dongen Jasper, van Swieten John C, Vandenberghe Rik, Vidal Jean-Sébastien, Visser Pieter J, Vogelgsang Jonathan, Waern Margda, Wagner Michael, Wiltfang Jens, Wittens Mandy M J, Zetterberg Henrik, Zulaica Miren, van Duijn Cornelia M, Bjerke Maria, Engelborghs Sebastiaan, Jessen Frank, Teunissen Charlotte E, Pastor Pau, Hiltunen Mikko, Ingelsson Martin, Andreassen Ole A, Clarimón Jordi, Sleegers Kristel, Ruiz Agustín, Ramirez Alfredo, Cruchaga Carlos, Lambert Jean-Charles, van der Flier Wies |
Sex-specific analysis in Behçet's disease reveals higher genetic risk in male patients. Journal of autoimmunity 2022 8 132 102882. Jo Yun Gun, Ortiz-Fernández Lourdes, Coit Patrick, Yilmaz Vuslat, Yentür Sibel P, Alibaz-Oner Fatma, Aksu Kenan, Erken Eren, Düzgün Nursen, Keser Gokhan, Cefle Ayse, Yazici Ayten, Ergen Andac, Alpsoy Erkan, Salvarani Carlo, K?sac?k Bünyamin, Kötter Ina, Henes Jörg, Ç?nar Muhammet, Schaefer Arne, Nohutcu Rahime M, Takeuchi Fujio, Harihara Shinji, Kaburaki Toshikatsu, Messedi Meriam, Song Yeong-Wook, Ka?ifo?lu Timuçin, Martin Javier, González Escribano María Francisca, Saruhan-Direskeneli Güher, Direskeneli Haner, Sawalha Amr |
Altered Thermal Behavior of Blood Plasma Proteome Related to Inflammatory Cytokines in Early Pregnancy Loss. International journal of molecular sciences 2022 Aug 23 (15): . Komsa-Penkova Regina, Danailova Avgustina, Krumova Sashka, Georgieva Galya, Giosheva Ina, Gartcheva Lidia, Iliev Ivan, Gartchev Emil, Kercheva Kameliya, Savov Alexey, Todinova Svet |
Implications of Decreased Expression of miR-125a with Respect to Its Variant Allele in the Pathogenesis of Recurrent Pregnancy Loss: A Study in a High Incidence Zone. Journal of clinical medicine 2022 Jul 11 (13): . Manzoor Usma, Pandith Arshad A, Amin Ina, Wani Saima, Sanadhya Dheera, Lone Tawseef A, Mir Hyder, Paray Bilal Ahamad, Gulnaz Aneela, Anwar Iqra, Ahmad Abida, Aein Qurat |
The Clinical Impact of Platelets on Post-Injury Serum Creatinine Concentration in Multiple Trauma Patients: A Retrospective Cohort Study. Medicina (Kaunas, Lithuania) 2022 7 58 (7): . Greve Frederik, Aulbach Ina, Mair Olivia, Biberthaler Peter, Hanschen Ma |
HLA class II variants defined by next generation sequencing are associated with sarcoidosis in Korean patients. Scientific reports 2022 Jun 12 (1): 9302. Sikorová Kate?ina, Moon Su-Jin, Yoon Hee-Young, Strnad Adam, Song Jin Woo, Petrek Mart |
Six genetically linked mutations in the CD36 gene significantly delay the onset of Alzheimer's disease. Scientific reports 2022 6 12 (1): 10994. Šerý Omar, Zeman Tomáš, Sheardová Kate?ina, Vyhnálek Martin, Marková Hana, Laczó Jan, Lochman Jan, Kralik Petr, Vrzalová Kamila, Dziedzinska Radka, Balcar Vladimir J, Hort Jak |
Mendelian Randomization Analysis Identifies Blood Tyrosine Levels as a Biomarker of Non-Alcoholic Fatty Liver Disease. Metabolites 2022 5 12 (5): . Gobeil Émilie, Maltais-Payette Ina, Taba Nele, Brière Francis, Ghodsian Nooshin, Abner Erik, Bourgault Jérôme, Gagnon Eloi, Manikpurage Hasanga D, Couture Christian, Mitchell Patricia L, Mathieu Patrick, Julien François, Corbeil Jacques, Vohl Marie-Claude, Thériault Sébastien, Esko Tõnu, Tchernof André, Arsenault Benoit |
Hematological Parameters in Individuals with Beta Thalassemia Trait in South Sumatra, Indonesia. Anemia 2022 5 2022 3572986. Sari Dian Puspita, Wahidiyat Pustika Amalia, Setianingsih Iswari, Timan Ina S, Gatot Djajadiman, Kekalih Ar |
NPM1 and DNMT3A mutations are associated with distinct blast immunophenotype in acute myeloid leukemia. Oncoimmunology 2022 5 11 (1): 2073050. Kuželová Kate?ina, Brodská Barbora, Marková Jana, Petrá?ková Martina, Schetelig Johannes, Ransdorfová Šárka, Gašová Zdenka, Šálek Cyr |
The effect of PARP inhibitors in homologous recombination proficient ovarian cancer: meta-analysis. Journal of chemotherapy (Florence, Italy) 2022 May 1-8. Skelin Marko, Šar?evi? David, Lešin Ga?ina Dina, Mucalo Iva, Dilber Ivo, Javor Eug |
Follicle Center Lymphoma (FCL) of the Lower Female Genital Tract (LFGT): A Novel Variant of Primary Cutaneous Follicle Center Lymphoma (PCFCL). The American journal of surgical pathology 2022 12 . Saksena Annapurna, Jain Ashish, Pack Svetlana D, Kim Jung, Lee Ina, Tyagi Manoj, Xi Liqiang, Pittaluga Stefania, Raffeld Mark, Jaffe Elaine |
Implications of risk conferred by 5p15.33 loci genetic variants; human telomerase reverse transcriptase rs2736098 and rs2736100 in predisposition of bladder cancer. Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology 2022 12 27 (5): 787-796. Anwar Iqra, Pandith Arshad A, Mir Hyder, Manzoor Usma, Amin Ina, Baba Shahid M, Godha Meena, Koul Aabid M, Shah Zafar A, Mansoor Sheikh, Wani Mohammad |
Common Genetic Variation and Age of Onset of Anorexia Nervosa.
Biological psychiatry global open science 2022 11 2 (4): 368-378. Watson Hunna J, Thornton Laura M, Yilmaz Zeynep, Baker Jessica H, Coleman Jonathan R I, Adan Roger A H, Alfredsson Lars, Andreassen Ole A, Ask Helga, Berrettini Wade H, Boehnke Michael, Boehm Ilka, Boni Claudette, Buehren Katharina, Bulant Josef, Burghardt Roland, Chang Xiao, Cichon Sven, Cone Roger D, Courtet Philippe, Crow Scott, Crowley James J, Danner Unna N, de Zwaan Martina, Dedoussis George, DeSocio Janiece E, Dick Danielle M, Dikeos Dimitris, Dina Christian, Djurovic Srdjan, Dmitrzak-Weglarz Monika, Docampo-Martinez Elisa, Duriez Philibert, Egberts Karin, Ehrlich Stefan, Eriksson Johan G, Escaramís Geòrgia, Esko Tõnu, Estivill Xavier, Farmer Anne, Fernández-Aranda Fernando, Fichter Manfred M, Föcker Manuel, Foretova Lenka, Forstner Andreas J, Frei Oleksandr, Gallinger Steven, Giegling Ina, Giuranna Johanna, Gonidakis Fragiskos, Gorwood Philip, Gratacòs Mònica, Guillaume Sébastien, Guo Yiran, Hakonarson Hakon, Hauser Joanna, Havdahl Alexandra, Hebebrand Johannes, Helder Sietske G, Herms Stefan, Herpertz-Dahlmann Beate, Herzog Wolfgang, Hinney Anke, Hübel Christopher, Hudson James I, Imgart Hartmut, Jamain Stephanie, Janout Vladimir, Jiménez-Murcia Susana, Jones Ian R, Julià Antonio, Kalsi Gursharan, Kaminská Deborah, Kaprio Jaakko, Karhunen Leila, Kas Martien J H, Keel Pamela K, Kennedy James L, Keski-Rahkonen Anna, Kiezebrink Kirsty, Klareskog Lars, Klump Kelly L, Knudsen Gun Peggy S, La Via Maria C, Le Hellard Stephanie, Leboyer Marion, Li Dong, Lilenfeld Lisa, Lin Bochao, Lissowska Jolanta, Luykx Jurjen, Magistretti Pierre, Maj Mario, Marsal Sara, Marshall Christian R, Mattingsdal Morten, Meulenbelt Ingrid, Micali Nadia, Mitchell Karen S, Monteleone Alessio Maria, Monteleone Palmiero, Myers Richard, Navratilova Marie, Ntalla Ionna, O'Toole Julie K, Ophoff Roel A, Padyukov Leonid, Pantel Jacques, Papežová Hana, Pinto Dalila, Raevuori Anu, Ramoz Nicolas, Reichborn-Kjennerud Ted, Ricca Valdo, Ripatti Samuli, Ripke Stephan, Ritschel Franziska, Roberts Marion, Rotondo Alessandro, Rujescu Dan, Rybakowski Filip, Scherag André, Scherer Stephen W, Schmidt Ulrike, Scott Laura J, Seitz Jochen, Silén Yasmina, Šlachtová Lenka, Slagboom P Eline, Slof-Op 't Landt Margarita C T, Slopien Agnieszka, Sorbi Sandro, ?wi?tkowska Beata, Tortorella Alfonso, Tozzi Federica, Treasure Janet, Tsitsika Artemis, Tyszkiewicz-Nwafor Marta, Tziouvas Konstantinos, van Elburg Annemarie A, van Furth Eric F, Walton Esther, Widen Elisabeth, Zerwas Stephanie, Zipfel Stephan, Bergen Andrew W, Boden Joseph M, Brandt Harry, Crawford Steven, Halmi Katherine A, Horwood L John, Johnson Craig, Kaplan Allan S, Kaye Walter H, Mitchell James E, Olsen Catherine M, Pearson John F, Pedersen Nancy L, Strober Michael, Werge Thomas, Whiteman David C, Woodside D Blake, Gordon Scott, Maguire Sarah, Larsen Janne T, Parker Richard, Petersen Liselotte V, Jordan Jennifer, Kennedy Martin, Wade Tracey D, Birgegård Andreas, Lichtenstein Paul, Landén Mikael, Martin Nicholas G, Mortensen Preben Bo, Breen Gerome, Bulik Cynthia |
NSCLC with uncommon EGFR mutations treated with atezolizumab plus bevacizumab and chemotherapy. Lung cancer (Amsterdam, Netherlands) 2022 11 174 141-145. Trummer Arne, Bethge Andre, Dickgreber Nicolas, Dittrich Ina, Golpon Heiko, Hoffknecht Petra, Overbeck Tobias R, Wesseler Claas, Reck Mart |
Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Molecular psychiatry 2022 10 27 (11): 4453-4463. Tielbeek Jorim J, Uffelmann Emil, Williams Benjamin S, Colodro-Conde Lucía, Gagnon Éloi, Mallard Travis T, Levitt Brandt E, Jansen Philip R, Johansson Ada, Sallis Hannah M, Pistis Giorgio, Saunders Gretchen R B, Allegrini Andrea G, Rimfeld Kaili, Konte Bettina, Klein Marieke, Hartmann Annette M, Salvatore Jessica E, Nolte Ilja M, Demontis Ditte, Malmberg Anni L K, Burt S Alexandra, Savage Jeanne E, Sugden Karen, Poulton Richie, Harris Kathleen Mullan, Vrieze Scott, McGue Matt, Iacono William G, Mota Nina Roth, Mill Jonathan, Viana Joana F, Mitchell Brittany L, Morosoli Jose J, Andlauer Till F M, Ouellet-Morin Isabelle, Tremblay Richard E, Côté Sylvana M, Gouin Jean-Philippe, Brendgen Mara R, Dionne Ginette, Vitaro Frank, Lupton Michelle K, Martin Nicholas G, , , Castelao Enrique, Räikkönen Katri, Eriksson Johan G, Lahti Jari, Hartman Catharina A, Oldehinkel Albertine J, Snieder Harold, Liu Hexuan, Preisig Martin, Whipp Alyce, Vuoksimaa Eero, Lu Yi, Jern Patrick, Rujescu Dan, Giegling Ina, Palviainen Teemu, Kaprio Jaakko, Harden Kathryn Paige, Munafò Marcus R, Morneau-Vaillancourt Geneviève, Plomin Robert, Viding Essi, Boutwell Brian B, Aliev Fazil, Dick Danielle M, Popma Arne, Faraone Stephen V, Børglum Anders D, Medland Sarah E, Franke Barbara, Boivin Michel, Pingault Jean-Baptiste, Glennon Jeffrey C, Barnes J C, Fisher Simon E, Moffitt Terrie E, Caspi Avshalom, Polderman Tinca J C, Posthuma Daniel |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
Clinical presentation and genetic variants in patients with autoinflammatory diseases: results from the German GARROD registry. Rheumatology international 2023 9 . Norbert Blank, Ina Kötter, Marc Schmalzing, Jürgen Rech, Karoline Krause, Birgit Köhler, Dorothee Kaudewitz, Martin Nitschke, Christian S Haas, Hanns-Martin Lorenz, Martin Krusc |
Germline variant of CTC1 gene in a patient with pulmonary fibrosis and myelodysplastic syndrome. Multidisciplinary respiratory medicine 2023 7 18 (1): 909. Martina Doubková, Zuzana Vrzalová, Marianna Štefániková, Libor ?ervinek, Kate?ina Sta?o Kozubík, Ivona Blaháková, Šárka Pospíšilová, Michael Doub |
Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants. American journal of medical genetics. Part A 2023 6 . Sheraz Khan, Ina Ofelia Foc?a, Magdalena Budi?teanu, Cristina Stoica, Florina Nedelea, Lauren?iu Bohîl?ea, Lavinia Caba, L?cr?mioara Butnariu, Monica Pânzaru, Cristina Rusu, Claudia Jurc?, Adela Chirita-Emandi, Claudia B?nescu, Wasim Abbas, Azita Sadeghpour, Shahid Mahmood Baig, Mihaela B?lgr?dean, Erica E Dav |
PTPN22 intron polymorphism rs1310182 (c.2054-852T>C) is associated with type 1 diabetes mellitus in patients of Armenian descent. PloS one 2023 6 18 (6): e0286743. Robert Žak, Lusine Navasardyan, Ján Hunák, Ji?ina Martin?, Petr Henebe |
Endometrial Carcinomas With Subclonal Loss of Mismatch Repair Proteins: A Clinicopathologic and Genomic Study. The American journal of surgical pathology 2023 3 . Mendoza Rachelle P, Wang Peng, Schulte Jefree J, Tjota Melissa Y, Jani Ina, Martinez Anna C, Haridas Rishikesh, Wanjari Pankhuri, Steinhardt George, Brown Noah, Betz Bryan L, Chapel David B, Kertowidjojo Elizabeth, Yamada S D, Bennett Jennifer |
Codon-specific KRAS mutations predict survival benefit of trifluridine/tipiracil in metastatic colorectal cancer. Nature medicine 2023 3 . van de Haar Joris, Ma Xuhui, Ooft Salo N, van der Helm Pim W, Hoes Louisa R, Mainardi Sara, Pinato David J, Sun Kristi, Salvatore Lisa, Tortora Giampaolo, Zurlo Ina Valeria, Leo Silvana, Giampieri Riccardo, Berardi Rossana, Gelsomino Fabio, Merz Valeria, Mazzuca Federica, Antonuzzo Lorenzo, Rosati Gerardo, Stavraka Chara, Ross Paul, Rodriquenz Maria Grazia, Pavarana Michele, Messina Carlo, Iveson Timothy, Zoratto Federica, Thomas Anne, Fenocchio Elisabetta, Ratti Margherita, Depetris Ilaria, Cergnul Massimiliano, Morelli Cristina, Libertini Michela, Parisi Alessandro, De Tursi Michele, Zanaletti Nicoletta, Garrone Ornella, Graham Janet, Longarini Raffaella, Gobba Stefania Maria, Petrillo Angelica, Tamburini Emiliano, La Verde Nicla, Petrelli Fausto, Ricci Vincenzo, Wessels Lodewyk F A, Ghidini Michele, Cortellini Alessio, Voest Emile E, Valeri Nico |
ApoE Alzheimer's Disease A?-amyloid plaque morphology varies according to APOE isotype. Research square 2023 2 . Caesar Ina, Nilsson K Peter R, Hammarstrom Per, Lindgren Mikael, Prokop Stefan, Heppner Frank L, Schmeidler James, Haroutunian Vahram, Holtzman David M, Hof Patrick R, Gandy S |
Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup. British journal of haematology 2023 11 . Senthilkumar Ramamoorthy, Dirk Lebrecht, Denny Schanze, Ina Schanze, Ilse Wieland, Geoffroy Andrieux, Patrick Metzger, Maria Hess, Michael H Albert, Arndt Borkhardt, Dorine Bresters, Jochen Buechner, Albert Catala, Valerie De Haas, Michael Dworzak, Miriam Erlacher, Henrik Hasle, Kirsi Jahnukainen, Franco Locatelli, Riccardo Masetti, Jan Stary, Dominik Turkiewicz, Luca Vinci, Marcin W Wlodarski, Ayami Yoshimi, Melanie Boerries, Charlotte M Niemeyer, Martin Zenker, Christian Flot |
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. The American journal of psychiatry 2023 10 180 (10): 723-738. Anna R Docherty, Niamh Mullins, Allison E Ashley-Koch, Xuejun Qin, Jonathan R I Coleman, Andrey Shabalin, JooEun Kang, Balasz Murnyak, Frank Wendt, Mark Adams, Adrian I Campos, Emily DiBlasi, Janice M Fullerton, Henry R Kranzler, Amanda V Bakian, Eric T Monson, Miguel E Rentería, Consuelo Walss-Bass, Ole A Andreassen, Chittaranjan Behera, Cynthia M Bulik, Howard J Edenberg, Ronald C Kessler, J John Mann, John I Nurnberger, Giorgio Pistis, Fabian Streit, Robert J Ursano, Renato Polimanti, Michelle Dennis, Melanie Garrett, Lauren Hair, Philip Harvey, Elizabeth R Hauser, Michael A Hauser, Jennifer Huffman, Daniel Jacobson, Ravi Madduri, Benjamin McMahon, David W Oslin, Jodie Trafton, Swapnil Awasthi, Wade H Berrettini, Martin Bohus, Xiao Chang, Hsi-Chung Chen, Wei J Chen, Erik D Christensen, Scott Crow, Philibert Duriez, Alexis C Edwards, Fernando Fernández-Aranda, Hanga Galfalvy, Michael Gandal, Philip Gorwood, Yiran Guo, Jonathan D Hafferty, Hakon Hakonarson, Katherine A Halmi, Akitoyo Hishimoto, Sonia Jain, Stéphane Jamain, Susana Jiménez-Murcia, Craig Johnson, Allan S Kaplan, Walter H Kaye, Pamela K Keel, James L Kennedy, Minsoo Kim, Kelly L Klump, Daniel F Levey, Dong Li, Shih-Cheng Liao, Klaus Lieb, Lisa Lilenfeld, Christian R Marshall, James E Mitchell, Satoshi Okazaki, Ikuo Otsuka, Dalila Pinto, Abigail Powers, Nicolas Ramoz, Stephan Ripke, Stefan Roepke, Vsevolod Rozanov, Stephen W Scherer, Christian Schmahl, Marcus Sokolowski, Anna Starnawska, Michael Strober, Mei-Hsin Su, Laura M Thornton, Janet Treasure, Erin B Ware, Hunna J Watson, Stephanie H Witt, D Blake Woodside, Zeynep Yilmaz, Lea Zillich, Rolf Adolfsson, Ingrid Agartz, Martin Alda, Lars Alfredsson, Vivek Appadurai, María Soler Artigas, Sandra Van der Auwera, M Helena Azevedo, Nicholas Bass, Claiton H D Bau, Bernhard T Baune, Frank Bellivier, Klaus Berger, Joanna M Biernacka, Tim B Bigdeli, Elisabeth B Binder, Michael Boehnke, Marco P Boks, David L Braff, Richard Bryant, Monika Budde, Enda M Byrne, Wiepke Cahn, Enrique Castelao, Jorge A Cervilla, Boris Chaumette, Aiden Corvin, Nicholas Craddock, Srdjan Djurovic, Jerome C Foo, Andreas J Forstner, Mark Frye, Justine M Gatt, Ina Giegling, Hans J Grabe, Melissa J Green, Eugenio H Grevet, Maria Grigoroiu-Serbanescu, Blanca Gutierrez, Jose Guzman-Parra, Marian L Hamshere, Annette M Hartmann, Joanna Hauser, Stefanie Heilmann-Heimbach, Per Hoffmann, Marcus Ising, Ian Jones, Lisa A Jones, Lina Jonsson, René S Kahn, John R Kelsoe, Kenneth S Kendler, Stefan Kloiber, Karestan C Koenen, Manolis Kogevinas, Marie-Odile Krebs, Mikael Landén, Marion Leboyer, Phil H Lee, Douglas F Levinson, Calwing Liao, Jolanta Lissowska, Fermin Mayoral, Susan L McElroy, Patrick McGrath, Peter McGuffin, Andrew McQuillin, Divya Mehta, Ingrid Melle, Philip B Mitchell, Esther Molina, Gunnar Morken, Caroline Nievergelt, Markus M Nöthen, Michael C O'Donovan, Roel A Ophoff, Michael J Owen, Carlos Pato, Michele T Pato, Brenda W J H Penninx, James B Potash, Robert A Power, Martin Preisig, Digby Quested, Josep Antoni Ramos-Quiroga, Andreas Reif, Marta Ribasés, Vanesa Richarte, Marcella Rietschel, Margarita Rivera, Andrea Roberts, Gloria Roberts, Guy A Rouleau, Diego L Rovaris, Alan R Sanders, Peter R Schofield, Thomas G Schulze, Laura J Scott, Alessandro Serretti, Jianxin Shi, Lea Sirignano, Pamela Sklar, Olav B Smeland, Jordan W Smoller, Edmund J S Sonuga-Barke, Maciej Trzaskowski, Ming T Tsuang, Gustavo Turecki, Laura Vilar-Ribó, John B Vincent, Henry Völzke, James T R Walters, Cynthia Shannon Weickert, Thomas W Weickert, Myrna M Weissman, Leanne M Williams, Naomi R Wray, Clement C Zai, Esben Agerbo, Anders D Børglum, Gerome Breen, Ditte Demontis, Annette Erlangsen, Joel Gelernter, Stephen J Glatt, David M Hougaard, Hai-Gwo Hwu, Po-Hsiu Kuo, Cathryn M Lewis, Qingqin S Li, Chih-Min Liu, Nicholas G Martin, Andrew M McIntosh, Sarah E Medland, Ole Mors, Merete Nordentoft, Catherine M Olsen, David Porteous, Daniel J Smith, Eli A Stahl, Murray B Stein, Danuta Wasserman, Thomas Werge, David C Whiteman, Virginia Willour, , , , , , , , , Hilary Coon, Jean C Beckham, Nathan A Kimbrel, Douglas M Ruderf |
Prognostic refinement of NSMP high-risk endometrial cancers using oestrogen receptor immunohistochemistry. British journal of cancer 2023 1 . Vermij Lisa, Jobsen Jan J, León-Castillo Alicia, Brinkhuis Mariel, Roothaan Suzan, Powell Melanie E, de Boer Stephanie M, Khaw Pearly, Mileshkin Linda R, Fyles Anthony, Leary Alexandra, Genestie Catherine, Jürgenliemk-Schulz Ina M, Crosbie Emma J, Mackay Helen J, Nijman Hans W, Nout Remi A, Smit Vincent T H B M, Creutzberg Carien L, Horeweg Nanda, Bosse Tjalling, |
Effect of NAT2, GSTM1 and CYP2E1 genetic polymorphisms on plasma concentration of isoniazid and its metabolites in patients with tuberculosis, and the assessment of exposure-response relationships. Frontiers in pharmacology 2024 4 15 1332752. Viktorija Ulanova, Agnija Kivrane, Anda Viksna, Leonora Pahirko, Lauma Freimane, Darja Sadovska, Iveta Ozere, Andra Cirule, Eduards Sevostjanovs, Solveiga Grinberga, Dace Bandere, Renate Ran |
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