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HPA axis in major depression: cortisol, clinical symptomatology and genetic variation predict cognition
HPA axis in major depression: cortisol, clinical symptomatology and genetic variation predict cognition
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HPA axis in major depression: cortisol, clinical symptomatology and genetic variation predict cognition

Keller, J ; Gomez, R ; Williams, G ; Lembke, A ; Lazzeroni, L ; Murphy, Jr, G M ; Schatzberg, A F

Molecular psychiatry, 2017-04, Vol.22 (4), p.527-536 [Periódico revisado por pares]

England: Nature Publishing Group

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2
High-resolution copy number variation analysis of schizophrenia in Japan
High-resolution copy number variation analysis of schizophrenia in Japan
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High-resolution copy number variation analysis of schizophrenia in Japan

Kushima, I ; Aleksic, B ; Nakatochi, M ; Shimamura, T ; Shiino, T ; Yoshimi, A ; Kimura, H ; Takasaki, Y ; Wang, C ; Xing, J ; Ishizuka, K ; Oya-Ito, T ; Nakamura, Y ; Arioka, Y ; Maeda, T ; Yamamoto, M ; Yoshida, M ; Noma, H ; Hamada, S ; Morikawa, M ; Uno, Y ; Okada, T ; Iidaka, T ; Iritani, S ; Yamamoto, T ; Miyashita, M ; Kobori, A ; Arai, M ; Itokawa, M ; Cheng, M-C ; Chuang, Y-A ; Chen, C-H ; Suzuki, M ; Takahashi, T ; Hashimoto, R ; Yamamori, H ; Yasuda, Y ; Watanabe, Y ; Nunokawa, A ; Someya, T ; Ikeda, M ; Toyota, T ; Yoshikawa, T ; Numata, S ; Ohmori, T ; Kunimoto, S ; Mori, D ; Iwata, N ; Ozaki, N

Molecular psychiatry, 2017-03, Vol.22 (3), p.430-440 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Evaluation of biological variation of glycated hemoglobin and glycated albumin in healthy Chinese subjects
Evaluation of biological variation of glycated hemoglobin and glycated albumin in healthy Chinese subjects
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Evaluation of biological variation of glycated hemoglobin and glycated albumin in healthy Chinese subjects

Liang, Libo ; He, He ; Zeng, Yuping ; Zhang, Mei ; Wang, Xia ; Li, Xiaoling ; Liang, Shanshan ; An, Zhenmei ; Huang, Hengjian

Journal of clinical laboratory analysis, 2019-03, Vol.33 (3), p.e22715-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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4
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

Huang, Alden Y. ; Yu, Dongmei ; Davis, Lea K. ; Sul, Jae Hoon ; Tsetsos, Fotis ; Ramensky, Vasily ; Zelaya, Ivette ; Ramos, Eliana Marisa ; Osiecki, Lisa ; Chen, Jason A. ; McGrath, Lauren M. ; Illmann, Cornelia ; Sandor, Paul ; Barr, Cathy L. ; Grados, Marco ; Singer, Harvey S. ; Nöthen, Markus M. ; Hebebrand, Johannes ; King, Robert A. ; Dion, Yves ; Rouleau, Guy ; Budman, Cathy L. ; Depienne, Christel ; Worbe, Yulia ; Hartmann, Andreas ; Müller-Vahl, Kirsten R. ; Stuhrmann, Manfred ; Aschauer, Harald ; Stamenkovic, Mara ; Schloegelhofer, Monika ; Konstantinidis, Anastasios ; Lyon, Gholson J. ; McMahon, William M. ; Barta, Csaba ; Tarnok, Zsanett ; Nagy, Peter ; Batterson, James R. ; Rizzo, Renata ; Cath, Danielle C. ; Wolanczyk, Tomasz ; Berlin, Cheston ; Malaty, Irene A. ; Okun, Michael S. ; Woods, Douglas W. ; Rees, Elliott ; Pato, Carlos N. ; Pato, Michele T. ; Knowles, James A. ; Posthuma, Danielle ; Pauls, David L. ; Cox, Nancy J. ; Neale, Benjamin M. ; Freimer, Nelson B. ; Paschou, Peristera ; Mathews, Carol A. ; Scharf, Jeremiah M. ; Coppola, Giovanni ; Bruun, Ruth D. ; Chouinard, Sylvain ; Darrow, Sabrina ; Greenberg, Erica ; Hirschtritt, Matthew E. ; Kurlan, Roger ; Leckman, James F. ; Robertson, Mary M. ; Smit, Jan

Neuron, 2017-06, Vol.94 (6), p.1101-1111.e7 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

Davies, Robert W ; Fiksinski, Ania M ; Breetvelt, Elemi J ; Williams, Nigel M ; Hooper, Stephen R ; Monfeuga, Thomas ; Bassett, Anne S ; Owen, Michael J ; Gur, Raquel E ; Morrow, Bernice E ; McDonald-McGinn, Donna M ; Swillen, Ann ; Chow, Eva W C ; van den Bree, Marianne ; Emanuel, Beverly S ; Vermeesch, Joris R ; van Amelsvoort, Therese ; Arango, Celso ; Armando, Marco ; Campbell, Linda E ; Cubells, Joseph F ; Eliez, Stephan ; Garcia-Minaur, Sixto ; Gothelf, Doron ; Kates, Wendy R ; Murphy, Kieran C ; Murphy, Clodagh M ; Murphy, Declan G ; Philip, Nicole ; Repetto, Gabriela M ; Shashi, Vandana ; Simon, Tony J ; Suñer, Damiàn Heine ; Vicari, Stefano ; Scherer, Stephen W ; Bearden, Carrie E ; Vorstman, Jacob A S

Nature Medicine, 2020-12, Vol.26 (12), p.1912-1918 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Bridging the Nomothetic and Idiographic Approaches to the Analysis of Clinical Data
Bridging the Nomothetic and Idiographic Approaches to the Analysis of Clinical Data
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Bridging the Nomothetic and Idiographic Approaches to the Analysis of Clinical Data

Beltz, Adriene M. ; Wright, Aidan G. C. ; Sprague, Briana N. ; Molenaar, Peter C. M. Hopwood, Christopher J ; Wright, Aidan G. C

Assessment (Odessa, Fla.), 2016-08, Vol.23 (4), p.447-458 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

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7
CNVs conferring risk of autism or schizophrenia affect cognition in controls
CNVs conferring risk of autism or schizophrenia affect cognition in controls
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CNVs conferring risk of autism or schizophrenia affect cognition in controls

Stefansson, Hreinn ; Meyer-Lindenberg, Andreas ; Steinberg, Stacy ; Magnusdottir, Brynja ; Morgen, Katrin ; Arnarsdottir, Sunna ; Bjornsdottir, Gyda ; Walters, G Bragi ; Jonsdottir, Gudrun A ; Doyle, Orla M ; Tost, Heike ; Grimm, Oliver ; Kristjansdottir, Solveig ; Snorrason, Heimir ; Davidsdottir, Solveig R ; Gudmundsson, Larus J ; Jonsson, Gudbjorn F ; Stefansdottir, Berglind ; Helgadottir, Isafold ; Haraldsson, Magnus ; Jonsdottir, Birna ; Thygesen, Johan H ; Schwarz, Adam J ; Didriksen, Michael ; Stensbøl, Tine B ; Brammer, Michael ; Kapur, Shitij ; Halldorsson, Jonas G ; Hreidarsson, Stefan ; Saemundsen, Evald ; Sigurdsson, Engilbert ; Stefansson, Kari

Nature (London), 2014-01, Vol.505 (7483), p.361-366 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Common genetic variants influence human subcortical brain structures
Common genetic variants influence human subcortical brain structures
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Common genetic variants influence human subcortical brain structures

Stein, Jason L ; Desrivières, Sylvane ; Toro, Roberto ; Armstrong, Nicola J ; Bernard, Manon ; Bralten, Janita ; Brown, Andrew A ; Ching, Christopher R K ; den Braber, Anouk ; Woldehawariat, Girma ; Janowitz, Deborah ; Jia, Tianye ; Lee, Phil H ; Macare, Christine ; Ramasamy, Adaikalavan ; Risacher, Shannon L ; Schmaal, Lianne ; Westlye, Lars T ; Athanasiu, Lavinia ; Hakobjan, Marina M H ; Haukvik, Unn K ; Heister, Angelien J G A M ; Hoehn, David ; Lopez, Lorna M ; Royle, Natalie A ; van Hulzen, Kimm J E ; Walton, Esther ; Ames, David ; Assareh, Amelia A ; Bastin, Mark E ; Corvin, Aiden ; de Zubicaray, Greig I ; Duggirala, Ravi ; Dyer, Thomas D ; Erk, Susanne ; Fedko, Iryna O ; Guelfi, Sebastian ; Hansell, Narelle K ; Hegenscheid, Katrin ; Heinz, Andreas ; Hoekstra, Pieter J ; Jenkinson, Mark ; Kent, Jr, Jack W ; Longo, Dan L ; Meisenzahl, Eva ; Melle, Ingrid ; Mohnke, Sebastian ; Mostert, Jeanette C ; Nalls, Michael A ; Nilsson, Lars G ; Reppermund, Simone ; Rujescu, Dan ; Schnell, Knut ; Steen, Vidar M ; Thalamuthu, Anbupalam ; Toga, Arthur W ; Troncoso, Juan ; van 't Ent, Dennis ; van der Brug, Marcel ; Veltman, Dick J ; Wassink, Thomas H ; Westman, Eric ; Zielke, Ronald H ; Ashbrook, David G ; Morris, Derek W ; Buckner, Randy L ; Dale, Anders M ; Delanty, Norman ; Kahn, René S ; Meyer-Lindenberg, Andreas ; Müller-Myhsok, Bertram ; Nyberg, Lars ; Sisodiya, Sanjay M ; van Bokhoven, Hans ; Völzke, Henry ; Weiner, Michael W ; Agartz, Ingrid ; Andreassen, Ole A ; Blangero, John ; Cannon, Dara M ; Deary, Ian J ; Fisher, Simon E ; Glahn, David C ; Grabe, Hans J ; Hulshoff Pol, Hilleke E ; Lovestone, Simon ; Mecocci, Patrizia ; McIntosh, Andrew M ; Ophoff, Roel A ; Ryten, Mina ; Wardlaw, Joanna M ; Schmidt, Reinhold ; Yanek, Lisa ; Greve, Douglas ; Nyquist, Paul ; Vinke, Louis N ; Mazoyer, Bernard ; Wright, Margaret J ; Schumann, Gunter ; Thompson, Paul M

Nature (London), 2015-04, Vol.520 (7546), p.224-229 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Patterns of de novo tandem repeat mutations and their role in autism
Patterns of de novo tandem repeat mutations and their role in autism
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Patterns of de novo tandem repeat mutations and their role in autism

Mitra, Ileena ; Huang, Bonnie ; Mousavi, Nima ; Ma, Nichole ; Lamkin, Michael ; Yanicky, Richard ; Shleizer-Burko, Sharona ; Lohmueller, Kirk E ; Gymrek, Melissa

Nature (London), 2021-01, Vol.589 (7841), p.246-250 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Molecular analysis of circulating tumor cells identifies distinct copy-number profiles in patients with chemosensitive and chemorefractory small-cell lung cancer
Molecular analysis of circulating tumor cells identifies distinct copy-number profiles in patients with chemosensitive and chemorefractory small-cell lung cancer
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Molecular analysis of circulating tumor cells identifies distinct copy-number profiles in patients with chemosensitive and chemorefractory small-cell lung cancer

Carter, Louise ; Rothwell, Dominic G ; Mesquita, Barbara ; Smowton, Christopher ; Leong, Hui Sun ; Fernandez-Gutierrez, Fabiola ; Li, Yaoyong ; Burt, Deborah J ; Antonello, Jenny ; Morrow, Christopher J ; Hodgkinson, Cassandra L ; Morris, Karen ; Priest, Lynsey ; Carter, Mathew ; Miller, Crispin ; Hughes, Andrew ; Blackhall, Fiona ; Dive, Caroline ; Brady, Ged

Nature medicine, 2017-01, Vol.23 (1), p.114-119 [Periódico revisado por pares]

United States: Nature Publishing Group

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