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- de Silva, Rohan
- Litvan, Irene
- Riley, David E
- van Swieten, John C
- Heutink, Peter
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Vandrovcova, Jana
- Hurtig, Howard I
- Gross, Rachel G
- Maetzler, Walter
- Goldwurm, Stefano
- Tolosa, Eduardo
- Borroni, Barbara
- Pastor, Pau
- Cantwell, Laura B
- Han, Mi Ryung
- Dillman, Allissa
- van der Brug, Marcel P
- Gibbs, J Raphael
- Cookson, Mark R
- Hernandez, Dena G
- Singleton, Andrew B
- Farrer, Matthew J
- Yu, Chang-En
- Golbe, Lawrence I
- Revesz, Tamas
- Hardy, John
- Lees, Andrew J
- Devlin, Bernie
- Hakonarson, Hakon
- Müller, Ulrich
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Probing the Virtual Proteome to Identify Novel Disease Biomarkers. [electronic resource] by
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- McCarty, Catherine A
- Chute, Christopher G
- Jarvik, Gail P
- Gordon, Adam S
- Palmer, Melody R
- Crosslin, David R
- Larson, Eric B
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- Peissig, Peggy L
- Brilliant, Murray H
- Kitchner, Terrie E
- Linneman, James G
- Namjou, Bahram
- Williams, Marc S
- Ritchie, Marylyn D
- Borthwick, Kenneth M
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- Mentch, Frank D
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- Karlson, Elizabeth W
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- Zhu, Yineng
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Corrigendum: An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder. [electronic resource] by
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- Belangero, Sintia Iole
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- Salum, Giovanni Abrahão
- Pan, Pedro Mario
- Moriyama, Tais Silveira
- Graeff-Martins, Ana Soledade
- Tamanaha, Ana Carina
- Alvarenga, Pedro
- Krieger, Fernanda Valle
- Fleitlich-Bilyk, Bacy
- Jackowski, Andrea Parolin
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- Sato, João Ricardo
- Polanczyk, Guilherme Vanoni
- Mari, Jair de Jesus
- Manfro, Gisele Gus
- do Rosário, Maria Conceição
- Miguel, Eurípedes Constantino
- Puga, Renato David
- Tahira, Ana Carolina
- Souza, Viviane Neri
- Chile, Thais
- Gouveia, Gisele Rodrigues
- Simões, Sérgio Nery
- Chang, Xiao
- Pellegrino, Renata
- Tian, Lifeng
- Glessner, Joseph T
- Hashimoto, Ronaldo Fumio
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Variants of DENND1B associated with asthma in children. [electronic resource] by
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- Michel, Sven
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- Zhang, Haitao
- Kim, Cecilia E
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- Glessner, Joseph T
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- Otieno, F George
- Santa, Erin
- Thomas, Kelly
- Smith, Ryan M
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- Beaty, Terri H
- Ruczinski, Ingo
- Orange, Jordan S
- Orange, Jordan M
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- Mathias, Rasika A
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- Li, Hongzhe
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A genome-wide association study on African-ancestry populations for asthma. [electronic resource] by
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- Maul, Pissamai
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- Sleiman, Patrick M A
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- Forno, Erick
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- Liang, Liming
- Abecasis, Gonçalo
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The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. [electronic resource] by
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- Chio, Adriano
- Dizdar, Nil
- Faltraco, Frank
- Forsgren, Lars
- Kirchheiner, Julia
- Kurz, Alexander
- Larsen, Jan P
- Liebsch, Maria
- Linder, Jan
- Morrison, Karen E
- Nissbrandt, Hans
- Otto, Markus
- Pahnke, Jens
- Partch, Amanda
- Restagno, Gabriella
- Rujescu, Dan
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- Tumani, Hayrettin
- Tysnes, Ole-Bjørn
- Valladares, Otto
- Silani, Vincenzo
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- Hakonarson, Hakon
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- Nguyen, Thomas A
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- Levin, Albert M
- Celedón, Juan C
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- Hakonarson, Hakon
- Sleiman, Patrick M
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- Brigino-Buenaventura, Emerita
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- Winkler, Cheryl A
- Moreno-Estrada, Andrés
- Sandoval, Karla
- Rodriguez-Santana, Jose R
- Kumar, Rajesh
- Williams, L Keoki
- Ahituv, Nadav
- Ziv, Elad
- Seibold, Max A
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Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. [electronic resource] by
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- Zubair, Niha
- Lu, Yingchang
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- Rasmussen-Torvik, Laura J
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- Sleiman, Patrick M
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- Correa, Adolfo
- Martin, Lisa W
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- Matise, Tara C
- Ambite, Jose Luis
- Carlson, Christopher S
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- Haiman, Chris
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Common genetic variants on 5p14.1 associate with autism spectrum disorders. [electronic resource] by
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- Bradfield, Jonathan P
- Sleiman, Patrick M A
- Kim, Cecilia E
- Hou, Cuiping
- Frackelton, Edward
- Chiavacci, Rosetta
- Takahashi, Nagahide
- Sakurai, Takeshi
- Rappaport, Eric
- Lajonchere, Clara M
- Munson, Jeffrey
- Estes, Annette
- Korvatska, Olena
- Piven, Joseph
- Sonnenblick, Lisa I
- Alvarez Retuerto, Ana I
- Herman, Edward I
- Dong, Hongmei
- Hutman, Ted
- Sigman, Marian
- Ozonoff, Sally
- Klin, Ami
- Owley, Thomas
- Sweeney, John A
- Brune, Camille W
- Cantor, Rita M
- Bernier, Raphael
- Gilbert, John R
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- Levy, Susan E
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- Nurnberger, John I
- Haines, Jonathan L
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- Buxbaum, Joseph D
- Dawson, Geraldine
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. [electronic resource] by
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- Kim, Cecilia E
- Wood, Shawn
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- Brune, Camille W
- Bradfield, Jonathan P
- Imielinski, Marcin
- Frackelton, Edward C
- Reichert, Jennifer
- Crawford, Emily L
- Munson, Jeffrey
- Sleiman, Patrick M A
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- Annaiah, Kiran
- Thomas, Kelly
- Hou, Cuiping
- Glaberson, Wendy
- Flory, James
- Otieno, Frederick
- Garris, Maria
- Soorya, Latha
- Klei, Lambertus
- Piven, Joseph
- Meyer, Kacie J
- Anagnostou, Evdokia
- Sakurai, Takeshi
- Game, Rachel M
- Rudd, Danielle S
- Zurawiecki, Danielle
- McDougle, Christopher J
- Davis, Lea K
- Miller, Judith
- Posey, David J
- Michaels, Shana
- Kolevzon, Alexander
- Silverman, Jeremy M
- Bernier, Raphael
- Levy, Susan E
- Schultz, Robert T
- Dawson, Geraldine
- Owley, Thomas
- McMahon, William M
- Wassink, Thomas H
- Sweeney, John A
- Nurnberger, John I
- Coon, Hilary
- Sutcliffe, James S
- Minshew, Nancy J
- Grant, Struan F A
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- Cook, Edwin H
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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. [electronic resource] by
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- Freitag, Christine M
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- Todorov, Alexandre A
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- Rothenberger, Aribert
- Franke, Barbara
- Mick, Eric O
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- Buitelaar, Jan
- Lesch, Klaus-Peter
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- Romanos, Jasmin
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- Meyer, Jobst
- Pálmason, Haukur
- Seitz, Christiane
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- Smalley, Susan L
- Biederman, Joseph
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- Asherson, Philip
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Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. [electronic resource] by
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- Brooks, William S
- Halliday, Glenda M
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- Gearing, Marla
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- Dickson, Dennis W
- Rademakers, Rosa
- Boeve, Bradley F
- Pickering-Brown, Stuart M
- Snowden, Julie
- van Swieten, John C
- Heutink, Peter
- Seelaar, Harro
- Murrell, Jill R
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- Moreno, Fermin
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- Frosch, Matthew P
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In:
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- Wei, Zhi
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- Cardinale, Christopher J
- Bakay, Marina
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- Maggadottir, S Melkorka
- Thomas, Kelly A
- Qui, Haijun
- Chiavacci, Rosetta M
- Kim, Cecilia E
- Wang, Fengxiang
- Snyder, James
- Flatø, Berit
- Førre, Øystein
- Denson, Lee A
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- Guthery, Stephen L
- Latiano, Anna
- Perez, Elena
- Resnick, Elena
- Strisciuglio, Caterina
- Staiano, Annamaria
- Miele, Erasmo
- Silverberg, Mark S
- Lie, Benedicte A
- Punaro, Marilynn
- Russell, Richard K
- Wilson, David C
- Dubinsky, Marla C
- Monos, Dimitri S
- Annese, Vito
- Munro, Jane E
- Wise, Carol
- Chapel, Helen
- Cunningham-Rundles, Charlotte
- Orange, Jordan S
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- Sullivan, Kathleen E
- Kugathasan, Subra
- Griffiths, Anne M
- Satsangi, Jack
- Grant, Struan F A
- Sleiman, Patrick M A
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- Polychronakos, Constantin
- Baldassano, Robert N
- Luning Prak, Eline T
- Ellis, Justine A
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- Maggadottir, S Melkorka
- Hou, Cuiping
- Abrams, Debra J
- Chang, Diana
- Gao, Feng
- Guo, Yiran
- Wei, Zhi
- Connolly, John J
- Cardinale, Christopher J
- Bakay, Marina
- Glessner, Joseph T
- Li, Dong
- Kao, Charlly
- Thomas, Kelly A
- Qiu, Haijun
- Chiavacci, Rosetta M
- Kim, Cecilia E
- Wang, Fengxiang
- Snyder, James
- Richie, Marylyn D
- Flatø, Berit
- Førre, Øystein
- Denson, Lee A
- Thompson, Susan D
- Becker, Mara L
- Guthery, Stephen L
- Latiano, Anna
- Perez, Elena
- Resnick, Elena
- Russell, Richard K
- Wilson, David C
- Silverberg, Mark S
- Annese, Vito
- Lie, Benedicte A
- Punaro, Marilynn
- Dubinsky, Marla C
- Monos, Dimitri S
- Strisciuglio, Caterina
- Staiano, Annamaria
- Miele, Erasmo
- Kugathasan, Subra
- Ellis, Justine A
- Munro, Jane E
- Sullivan, Kathleen E
- Wise, Carol A
- Chapel, Helen
- Cunningham-Rundles, Charlotte
- Grant, Struan F A
- Orange, Jordan S
- Sleiman, Patrick M A
- Behrens, Edward M
- Griffiths, Anne M
- Satsangi, Jack
- Finkel, Terri H
- Keinan, Alon
- Prak, Eline T Luning
- Polychronakos, Constantin
- Baldassano, Robert N
- Li, Hongzhe
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A genome-wide association meta-analysis identifies new childhood obesity loci. [electronic resource] by
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- Valcarcel, Beatriz
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- Jarick, Ivonne
- Pennell, Craig E
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- Berry, Diane J
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- Hofman, Albert
- Rivadeneira, Fernando
- Uitterlinden, André G
- van Duijn, Cornelia M
- van der Valk, Ralf J P
- de Jongste, Johan C
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- Lehtimäki, Terho
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- Das, Shikta
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- Bisgaard, Hans
- Gilliland, Frank D
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- Wheeler, Eleanor
- Barroso, Inês
- O'Rahilly, Stephen
- Meirhaeghe, Aline
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- Palmer, Lyle J
- Hinney, Anke
- Widen, Elisabeth
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- Hebebrand, Johannes
- Jarvelin, Marjo-Riitta
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. [electronic resource] by
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- van Swieten, John C
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In:
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In:
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- Søndergaard, Helle Bach
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- Syvänen, Ann-Christine
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In:
Nature vol. 476
Availability: No items available.
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