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Toward Genetic Prediction of Nonalcoholic Fatty Liver Disease Trajectories: PNPLA3 and Beyond
Toward Genetic Prediction of Nonalcoholic Fatty Liver Disease Trajectories: PNPLA3 and Beyond
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Toward Genetic Prediction of Nonalcoholic Fatty Liver Disease Trajectories: PNPLA3 and Beyond

Krawczyk, Marcin ; Liebe, Roman ; Lammert, Frank

Gastroenterology (New York, N.Y. 1943), 2020-05, Vol.158 (7), p.1865-1880.e1 [Periódico revisado por pares]

United States: Elsevier Inc

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Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction
Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction
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Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction

AYALEW, M ; LE-NICULESCU, H ; KOLLER, D ; NURNBERGER, J. I ; CORVIN, A ; GEYER, M ; TSUANG, M. T ; SALOMON, D ; SCHORK, N. J ; FANOUS, A. H ; O'DONOVAN, M. C ; NICULESCU, A. B ; LEVEY, D. F ; JAIN, N ; CHANGALA, B ; PATEL, S. D ; WINIGER, E ; BREIER, A ; SHEKHAR, A ; AMDUR, R

Molecular psychiatry, 2012-09, Vol.17 (9), p.887-905 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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3
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

Chauhan, Ganesh ; Arnold, Corey R ; Chu, Audrey Y ; Reyahi, Azadeh ; Bis, Joshua C ; Havulinna, Aki S ; Trompet, Stella ; Manichaikul, Ani ; Teumer, Alexander ; Gustafsson, Stefan ; Bartz, Traci M ; Bellenguez, Céline ; Vidal, Jean Sebastien ; Kjartansson, Olafur ; Satizabal, Claudia L ; Xue, Flora ; Liu, Yongmei ; Bevan, Steve ; Hopewell, Jemma C ; Heckbert, Susan R ; Rice, Kenneth ; Smith, Nicholas L ; Levi, Christopher ; Sharma, Pankaj ; Sudlow, Cathie LM ; Cole, John W ; Schmidt, Reinhold ; Meschia, James ; Thijs, Vincent ; Melander, Olle ; Grewal, Raji P ; Sacco, Ralph L ; Rundek, Tatjana ; Rothwell, Peter M ; Jern, Christina ; Johnson, Julie A ; Benavente, Oscar R ; Lee, Jin-Moo ; Wong, Quenna ; Aparicio, Hugo J ; Engelter, Stefan T ; Kloss, Manja ; Pezzini, Alessandro ; Buring, Julie E ; Ridker, Paul M ; Berr, Claudine ; Dartigues, Jean-François ; Hamsten, Anders ; Traylor, Matthew ; Pedersen, Nancy L ; Lannfelt, Lars ; Morris, Andrew P ; Jimenez-Conde, Jordi ; Montaner, Joan ; Slowik, Agnieszka ; Woo, Daniel ; Hofman, Albert ; Koudstaal, Peter J ; Portegies, Marileen L P ; Uitterlinden, André G ; Ford, Ian ; Jukema, J Wouter ; Stott, David J ; Allen, Norrina B ; Johnson, Andrew D ; De Jager, Philip L ; White, Charles C ; Markus, Marcello Ricardo Paulista ; Schminke, Ulf ; Boncoraglio, Giorgio B ; Clarke, Robert ; Kamatani, Yoichiro ; Dallongeville, Jean ; Rotter, Jerome I ; Nalls, Michael A ; Griswold, Michael E ; Knopman, David S ; Windham, B Gwen ; Beiser, Alexa ; Vartiainen, Erkki ; French, Curtis R ; Pastinen, Tomi ; Gudnason, Vilmundur ; Kurth, Tobias ; Harris, Tamara B ; Rich, Stephen S ; deStefano, Anita L ; Rosand, Jonathan ; Mosley, Thomas H ; Ingelsson, Erik ; van Duijn, Cornelia M ; Tzourio, Christophe ; Rexrode, Kathryn M ; Lehmann, Ordan J ; Launer, Lenore J ; Carlsson, Peter ; Chasman, Daniel I ; Childs, Sarah J ; Seshadri, Sudha ; Debette, Stéphanie

Lancet neurology, 2016-06, Vol.15 (7), p.695-707 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Bin1 directly remodels actin dynamics through its BAR domain
Bin1 directly remodels actin dynamics through its BAR domain
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Bin1 directly remodels actin dynamics through its BAR domain

Dräger, Nina M ; Nachman, Eliana ; Winterhoff, Moritz ; Brühmann, Stefan ; Shah, Pranav ; Katsinelos, Taxiarchis ; Boulant, Steeve ; Teleman, Aurelio A ; Faix, Jan ; Jahn, Thomas R

EMBO reports, 2017-11, Vol.18 (11), p.2051-2066 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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5
TREM2 in Neurodegenerative Diseases
TREM2 in Neurodegenerative Diseases
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TREM2 in Neurodegenerative Diseases

Jay, Taylor R ; von Saucken, Victoria E ; Landreth, Gary E

Molecular neurodegeneration, 2017-08, Vol.12 (1), p.56-56, Article 56 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant
TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant
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TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant

Thornton, Peter ; Sevalle, Jean ; Deery, Michael J ; Fraser, Graham ; Zhou, Ye ; Ståhl, Sara ; Franssen, Elske H ; Dodd, Roger B ; Qamar, Seema ; Gomez Perez‐Nievas, Beatriz ; Nicol, Louise SC ; Eketjäll, Susanna ; Revell, Jefferson ; Jones, Clare ; Billinton, Andrew ; St George‐Hyslop, Peter H ; Chessell, Iain ; Crowther, Damian C

EMBO molecular medicine, 2017-10, Vol.9 (10), p.1366-1378 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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7
Reliability of Genomic Predictions Across Multiple Populations
Reliability of Genomic Predictions Across Multiple Populations
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Reliability of Genomic Predictions Across Multiple Populations

Roos, A.P.W. de ; Hayes, B.J ; Goddard, M.E

Genetics (Austin), 2009-12, Vol.183 (4), p.1545-1553 [Periódico revisado por pares]

United States: Genetics Soc America

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8
Human complement factor H Y402H polymorphism causes an age-related macular degeneration phenotype and lipoprotein dysregulation in mice
Human complement factor H Y402H polymorphism causes an age-related macular degeneration phenotype and lipoprotein dysregulation in mice
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Human complement factor H Y402H polymorphism causes an age-related macular degeneration phenotype and lipoprotein dysregulation in mice

Landowski, Michael ; Kelly, Una ; Klingeborn, Mikael ; Groelle, Marybeth ; Ding, Jin-Dong ; Grigsby, Daniel ; Rickman, Catherine Bowes

Proceedings of the National Academy of Sciences - PNAS, 2019-02, Vol.116 (9), p.3703-3711 [Periódico revisado por pares]

United States: National Academy of Sciences

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9
Harnessing Genetic Complexity to Enhance Translatability of Alzheimer’s Disease Mouse Models: A Path toward Precision Medicine
Harnessing Genetic Complexity to Enhance Translatability of Alzheimer’s Disease Mouse Models: A Path toward Precision Medicine
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Harnessing Genetic Complexity to Enhance Translatability of Alzheimer’s Disease Mouse Models: A Path toward Precision Medicine

Neuner, Sarah M. ; Heuer, Sarah E. ; Huentelman, Matthew J. ; O’Connell, Kristen M.S. ; Kaczorowski, Catherine C.

Neuron (Cambridge, Mass.), 2019-02, Vol.101 (3), p.399-411.e5 [Periódico revisado por pares]

United States: Elsevier Inc

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10
The neurobiological basis of cognitive impairment in Parkinson's disease
The neurobiological basis of cognitive impairment in Parkinson's disease
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The neurobiological basis of cognitive impairment in Parkinson's disease

Halliday, Glenda M. ; Leverenz, James B. ; Schneider, Jay S. ; Adler, Charles H.

Movement disorders, 2014-04, Vol.29 (5), p.634-650 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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