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1
Age at first birth in women is genetically associated with increased risk of schizophrenia
Age at first birth in women is genetically associated with increased risk of schizophrenia
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Age at first birth in women is genetically associated with increased risk of schizophrenia

Ni, Guiyan ; Gratten, Jacob ; Wray, Naomi R ; Lee, Sang Hong

Scientific reports, 2018-07, Vol.8 (1), p.10168-14, Article 10168 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Anxiety and depression from age 3 to 8 years in children with and without ADHD symptoms
Anxiety and depression from age 3 to 8 years in children with and without ADHD symptoms
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Anxiety and depression from age 3 to 8 years in children with and without ADHD symptoms

Ingeborgrud, Christine Baalsrud ; Oerbeck, Beate ; Friis, Svein ; Zeiner, Pål ; Pripp, Are Hugo ; Aase, Heidi ; Biele, Guido ; Dalsgaard, Søren ; Overgaard, Kristin Romvig

Scientific reports, 2023-09, Vol.13 (1), p.15376-15376, Article 15376 [Periódico revisado por pares]

London: Nature Publishing Group

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3
Apparent diffusion coefficient estimates based on 24 hours tracer movement support glymphatic transport in human cerebral cortex
Apparent diffusion coefficient estimates based on 24 hours tracer movement support glymphatic transport in human cerebral cortex
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Apparent diffusion coefficient estimates based on 24 hours tracer movement support glymphatic transport in human cerebral cortex

Valnes, Lars Magnus ; Mitusch, Sebastian K ; Ringstad, Geir ; Eide, Per Kristian ; Funke, Simon W ; Mardal, Kent-Andre

Scientific reports, 2020-06, Vol.10 (1), p.9176-9176, Article 9176 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder
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Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

Gudmundsson, Olafur O ; Walters, G Bragi ; Ingason, Andres ; Johansson, Stefan ; Zayats, Tetyana ; Athanasiu, Lavinia ; Sonderby, Ida Elken ; Gustafsson, Omar ; Nawaz, Muhammad S ; Jonsson, Gudbjorn F ; Jonsson, Lina ; Knappskog, Per-Morten ; Ingvarsdottir, Ester ; Davidsdottir, Katrin ; Djurovic, Srdjan ; Knudsen, Gun Peggy Strømstad ; Askeland, Ragna Bugge ; Haraldsdottir, Gyda S ; Baldursson, Gisli ; Magnusson, Pall ; Sigurdsson, Engilbert ; Gudbjartsson, Daniel F ; Stefansson, Hreinn ; Andreassen, Ole A ; Haavik, Jan ; Reichborn-Kjennerud, Ted ; Stefansson, Kari

Translational psychiatry, 2019-10, Vol.9 (1), p.258-9, Article 258 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Automatic detection of valve events by epicardial accelerometer allows estimation of the left ventricular pressure trace and pressure-displacement loop area
Automatic detection of valve events by epicardial accelerometer allows estimation of the left ventricular pressure trace and pressure-displacement loop area
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Automatic detection of valve events by epicardial accelerometer allows estimation of the left ventricular pressure trace and pressure-displacement loop area

Wajdan, Ali ; Krogh, Magnus Reinsfelt ; Villegas-Martinez, Manuel ; Halvorsen, Per Steinar ; Elle, Ole Jakob ; Remme, Espen Wattenberg

Scientific reports, 2020-11, Vol.10 (1), p.20088-20088, Article 20088 [Periódico revisado por pares]

England: Nature Publishing Group UK

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6
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis
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Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis

Tønne, Elin ; Due-Tønnessen, Bernt Johan ; Mero, Inger-Lise ; Wiig, Ulrikke Straume ; Kulseth, Mari Ann ; Vigeland, Magnus Dehli ; Sheng, Ying ; von der Lippe, Charlotte ; Tveten, Kristian ; Meling, Torstein Ragnar ; Helseth, Eirik ; Heimdal, Ketil Riddervold

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.920-929 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Dominguez-Valentin, Mev ; Sampson, Julian R ; Seppälä, Toni T ; Ten Broeke, Sanne W ; Plazzer, John-Paul ; Nakken, Sigve ; Engel, Christoph ; Aretz, Stefan ; Jenkins, Mark A ; Sunde, Lone ; Bernstein, Inge ; Capella, Gabriel ; Balaguer, Francesc ; Thomas, Huw ; Evans, D Gareth ; Burn, John ; Greenblatt, Marc ; Hovig, Eivind ; de Vos Tot Nederveen Cappel, Wouter H ; Sijmons, Rolf H ; Bertario, Lucio ; Tibiletti, Maria Grazia ; Cavestro, Giulia Martina ; Lindblom, Annika ; Della Valle, Adriana ; Lopez-Köstner, Francisco ; Gluck, Nathan ; Katz, Lior H ; Heinimann, Karl ; Vaccaro, Carlos A ; Büttner, Reinhard ; Görgens, Heike ; Holinski-Feder, Elke ; Morak, Monika ; Holzapfel, Stefanie ; Hüneburg, Robert ; Knebel Doeberitz, Magnus von ; Loeffler, Markus ; Rahner, Nils ; Schackert, Hans K ; Steinke-Lange, Verena ; Schmiegel, Wolff ; Vangala, Deepak ; Pylvänäinen, Kirsi ; Renkonen-Sinisalo, Laura ; Hopper, John L ; Win, Aung Ko ; Haile, Robert W ; Lindor, Noralane M ; Gallinger, Steven ; Le Marchand, Loïc ; Newcomb, Polly A ; Figueiredo, Jane C ; Thibodeau, Stephen N ; Wadt, Karin ; Therkildsen, Christina ; Okkels, Henrik ; Ketabi, Zohreh ; Moreira, Leticia ; Sánchez, Ariadna ; Serra-Burriel, Miquel ; Pineda, Marta ; Navarro, Matilde ; Blanco, Ignacio ; Green, Kate ; Lalloo, Fiona ; Crosbie, Emma J ; Hill, James ; Denton, Oliver G ; Frayling, Ian M ; Rødland, Einar Andreas ; Vasen, Hans ; Mints, Miriam ; Neffa, Florencia ; Esperon, Patricia ; Alvarez, Karin ; Kariv, Revital ; Rosner, Guy ; Pinero, Tamara Alejandra ; Gonzalez, María Laura ; Kalfayan, Pablo ; Tjandra, Douglas ; Winship, Ingrid M ; Macrae, Finlay ; Möslein, Gabriela ; Mecklin, Jukka-Pekka ; Nielsen, Maartje ; Møller, Pål

Genetics in medicine, 2020-01, Vol.22 (1), p.15-25 [Periódico revisado por pares]

United States: Elsevier Limited

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8
Characterization of the genetic architecture of infant and early childhood body mass index
Characterization of the genetic architecture of infant and early childhood body mass index
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Characterization of the genetic architecture of infant and early childhood body mass index

Helgeland, Øyvind ; Vaudel, Marc ; Sole-Navais, Pol ; Flatley, Christopher ; Juodakis, Julius ; Bacelis, Jonas ; Koløen, Ingvild L ; Knudsen, Gun Peggy ; Johansson, Bente B ; Magnus, Per ; Kjennerud, Ted Reichborn ; Juliusson, Petur B ; Stoltenberg, Camilla ; Holmen, Oddgeir L ; Andreassen, Ole A ; Jacobsson, Bo ; Njølstad, Pål R ; Johansson, Stefan

Nature metabolism, 2022-03, Vol.4 (3), p.344-358 [Periódico revisado por pares]

Germany: Nature Portfolio

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9
Circulating small non-coding RNAs associated with age, sex, smoking, body mass and physical activity
Circulating small non-coding RNAs associated with age, sex, smoking, body mass and physical activity
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Circulating small non-coding RNAs associated with age, sex, smoking, body mass and physical activity

Rounge, Trine B ; Umu, Sinan U ; Keller, Andreas ; Meese, Eckart ; Ursin, Giske ; Tretli, Steinar ; Lyle, Robert ; Langseth, Hilde

Scientific reports, 2018-12, Vol.8 (1), p.17650-13, Article 17650 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Common variant at 16p11.2 conferring risk of psychosis
Common variant at 16p11.2 conferring risk of psychosis
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Common variant at 16p11.2 conferring risk of psychosis

Steinberg, S ; Mattheisen, M ; Costas, J ; Demontis, D ; Jamain, S ; Lin, K ; Papiol, S ; Huttenlocher, J ; Sigurdsson, E ; Vassos, E ; Giegling, I ; Breuer, R ; Fraser, G ; Walker, N ; Djurovic, S ; Agartz, I ; Suvisaari, J ; Paunio, T ; Olsen, L ; Hansen, T ; Ingason, A ; Pirinen, M ; Strengman, E ; Hougaard, D M ; Didriksen, M ; Kaleda, V ; Arango, C ; Bellivier, F ; Méary, A ; Schürhoff, F ; Szoke, A ; Ribolsi, M ; Rossner, M ; Kiemeney, L A ; Franke, B ; van den Berg, L H ; Veldink, J ; Curran, S ; Bolton, P ; Staal, W ; Rehnstrom, K ; Kilpinen, H ; Freitag, C M ; Meyer, J ; Magnusson, P ; Saemundsen, E ; Martsenkovsky, I ; Bikshaieva, I ; Martsenkovska, I ; Vashchenko, O ; Raleva, M ; Paketchieva, K ; Stefanovski, B ; Durmishi, N ; Lecic Tosevski, D ; Silagadze, T ; Naneishvili, N ; Mikeladze, N ; Vincent, J B ; Farmer, A ; Mitchell, P B ; Fullerton, J M ; Montgomery, G W ; Martin, N G ; Rubino, I A ; van Winkel, R ; Kenis, G ; De Hert, M ; Réthelyi, J M ; Bitter, I ; Jönsson, E G ; Jablensky, A ; Leboyer, M ; Bramon, E ; Powell, J ; Corvin, A ; Gill, M ; Morris, D ; O'Neill, F A ; Riley, B ; Craddock, N ; Owen, M J ; O'Donovan, M C ; Thorsteinsdottir, U ; Kong, A ; Carracedo, A ; Golimbet, V ; Børglum, A D ; Mors, O ; Mortensen, P B ; Ophoff, R A ; Nöthen, M M ; Cichon, S ; Ruggeri, M ; Tosato, S ; Palotie, A ; Rujescu, D ; Collier, D A ; Stefansson, H ; Stefansson, K

Molecular psychiatry, 2014-01, Vol.19 (1), p.108-114 [Periódico revisado por pares]

England: Nature Publishing Group

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