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Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. [electronic resource] by
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- Warnstedt, Maike
- Alekov, Alexi K
- Sander, Thomas
- Ramírez, Alfredo
- Poser, Barbara
- Maljevic, Snezana
- Hebeisen, Simon
- Kubisch, Christian
- Rebstock, Johannes
- Horvath, Steve
- Hallmann, Kerstin
- Dullinger, Joern S
- Rau, Birgit
- Haverkamp, Fritz
- Beyenburg, Stefan
- Schulz, Herbert
- Janz, Dieter
- Giese, Bernd
- Müller-Newen, Gerhard
- Propping, Peter
- Elger, Christian E
- Fahlke, Christoph
- Lerche, Holger
Producer: 20090928
In:
Nature genetics vol. 41
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102.
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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants. [electronic resource] by
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- Rodhe, Johanna
- Nesbitt, Ryan R
- Boyle, Evan A
- Martin, Beth K
- Lord, Jenny
- Karaca, Ilker
- Naj, Adam
- Jessen, Frank
- Helisalmi, Seppo
- Soininen, Hilkka
- Hiltunen, Mikko
- Ramirez, Alfredo
- Scherer, Martin
- Farrer, Lindsay A
- Haines, Jonathan L
- Pericak-Vance, Margaret A
- Raskind, Wendy H
- Cruchaga, Carlos
- Schellenberg, Gerard D
- Joseph, Bertrand
- Brkanac, Zoran
Producer: 20171019
In:
PloS one vol. 12
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Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulation. [electronic resource] by
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- Müller, Tobias
- Lardenoije, Roy
- Maierhofer, Anna
- Dittrich, Marcus
- Riemens, Renzo J M
- Stora, Samantha
- Roche, Mathilde
- Leber, Markus
- Riedel-Heller, Steffi
- Wagner, Michael
- Scherer, Martin
- Ravel, Aimé
- Mircher, Clotilde
- Cieuta-Walti, Cecile
- Durand, Sophie
- van de Hove, Daniel L A
- Hoffmann, Per
- Ramirez, Alfredo
- Haaf, Thomas
- El Hajj, Nady
- Mégarbané, André
Producer: 20200724
In:
Clinical epigenetics vol. 11
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104.
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A bistable circuit involving SCARECROW-RETINOBLASTOMA integrates cues to inform asymmetric stem cell division. [electronic resource] by
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- Díaz-Triviño, Sara
- Blilou, Ikram
- Grieneisen, Verônica A
- Sozzani, Rosangela
- Zamioudis, Christos
- Miskolczi, Pál
- Nieuwland, Jeroen
- Benjamins, René
- Dhonukshe, Pankaj
- Caballero-Pérez, Juan
- Horvath, Beatrix
- Long, Yuchen
- Mähönen, Ari Pekka
- Zhang, Hongtao
- Xu, Jian
- Murray, James A H
- Benfey, Philip N
- Bako, Laszlo
- Marée, Athanasius F M
- Scheres, Ben
Producer: 20121105
In:
Cell vol. 150
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105.
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Genetic interaction of PICALM and APOE is associated with brain atrophy and cognitive impairment in Alzheimer's disease. [electronic resource] by
- Morgen, Katrin
- Ramirez, Alfredo
- Frölich, Lutz
- Tost, Heike
- Plichta, Michael M
- Kölsch, Heike
- Rakebrandt, Fabian
- Rienhoff, Otto
- Jessen, Frank
- Peters, Oliver
- Jahn, Holger
- Luckhaus, Christian
- Hüll, Michael
- Gertz, Hermann-Josef
- Schröder, Johannes
- Hampel, Harald
- Teipel, Stefan J
- Pantel, Johannes
- Heuser, Isabella
- Wiltfang, Jens
- Rüther, Eckart
- Kornhuber, Johannes
- Maier, Wolfgang
- Meyer-Lindenberg, Andreas
Producer: 20150713
In:
Alzheimer's & dementia : the journal of the Alzheimer's Association vol. 10
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106.
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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. [electronic resource] by
- Haug, Karsten
- Warnstedt, Maike
- Alekov, Alexi K
- Sander, Thomas
- Ramírez, Alfredo
- Poser, Barbara
- Maljevic, Snezana
- Hebeisen, Simon
- Kubisch, Christian
- Rebstock, Johannes
- Horvath, Steve
- Hallmann, Kerstin
- Dullinger, Joern S
- Rau, Birgit
- Haverkamp, Fritz
- Beyenburg, Stefan
- Schulz, Herbert
- Janz, Dieter
- Giese, Bernd
- Müller-Newen, Gerhard
- Propping, Peter
- Elger, Christian E
- Fahlke, Christoph
- Lerche, Holger
- Heils, Armin
Producer: 20030516
In:
Nature genetics vol. 33
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107.
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Common polygenic variation enhances risk prediction for Alzheimer's disease. [electronic resource] by
- Escott-Price, Valentina
- Sims, Rebecca
- Bannister, Christian
- Harold, Denise
- Vronskaya, Maria
- Majounie, Elisa
- Badarinarayan, Nandini
- Morgan, Kevin
- Passmore, Peter
- Holmes, Clive
- Powell, John
- Brayne, Carol
- Gill, Michael
- Mead, Simon
- Goate, Alison
- Cruchaga, Carlos
- Lambert, Jean-Charles
- van Duijn, Cornelia
- Maier, Wolfgang
- Ramirez, Alfredo
- Holmans, Peter
- Jones, Lesley
- Hardy, John
- Seshadri, Sudha
- Schellenberg, Gerard D
- Amouyel, Philippe
- Williams, Julie
Producer: 20160504
In:
Brain : a journal of neurology vol. 138
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108.
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CLCN2 variants in idiopathic generalized epilepsy. [electronic resource] by
- Kleefuss-Lie, Ailing
- Friedl, Waltraut
- Cichon, Sven
- Haug, Karsten
- Warnstedt, Maike
- Alekov, Alexi
- Sander, Thomas
- Ramirez, Alfredo
- Poser, Barbara
- Maljevic, Snezana
- Hebeisen, Simon
- Kubisch, Christian
- Rebstock, Johannes
- Horvath, Steve
- Hallmann, Kerstin
- Dullinger, Jörn S
- Rau, Birgit
- Haverkamp, Fritz
- Beyenburg, Stefan
- Schulz, Herbert
- Janz, Dieter
- Giese, Bernd
- Müller-Newen, Gerhard
- Propping, Peter
- Elger, Christian E
- Fahlke, Christoph
- Lerche, Holger
Producer: 20090928
In:
Nature genetics vol. 41
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109.
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Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer. [electronic resource] by
- Neidhardt, Guido
- Hauke, Jan
- Ramser, Juliane
- Groß, Eva
- Gehrig, Andrea
- Müller, Clemens R
- Kahlert, Anne-Karin
- Hackmann, Karl
- Honisch, Ellen
- Niederacher, Dieter
- Heilmann-Heimbach, Stefanie
- Franke, André
- Lieb, Wolfgang
- Thiele, Holger
- Altmüller, Janine
- Nürnberg, Peter
- Klaschik, Kristina
- Ernst, Corinna
- Ditsch, Nina
- Jessen, Frank
- Ramirez, Alfredo
- Wappenschmidt, Barbara
- Engel, Christoph
- Rhiem, Kerstin
- Meindl, Alfons
- Schmutzler, Rita K
- Hahnen, Eric
Producer: 20170928
In:
JAMA oncology vol. 3
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110.
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Genome-wide significant risk factors on chromosome 19 and the [electronic resource] by
- Moreno-Grau, Sonia
- Hernández, Isabel
- Heilmann-Heimbach, Stefanie
- Ruiz, Susana
- Rosende-Roca, Maitée
- Mauleón, Ana
- Vargas, Liliana
- Rodríguez-Gómez, Octavio
- Alegret, Montserrat
- Espinosa, Ana
- Ortega, Gemma
- Aguilera, Nuria
- Abdelnour, Carla
- Neuroimaging Initiative, Alzheimer's Disease
- Gil, Silvia
- Maier, Wolfgang
- Sotolongo-Grau, Oscar
- Tárraga, Lluís
- Ramirez, Alfredo
- López-Arrrieta, Jesús
- Antúnez, Carmen
- Serrano-Ríos, Manuel
- Boada, Mercè
- Ruiz, Agustín
Publication details: Oncotarget May 2018
In:
Oncotarget vol. 9
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111.
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Design and first baseline data of the DZNE multicenter observational study on predementia Alzheimer's disease (DELCODE). [electronic resource] by
- Jessen, Frank
- Spottke, Annika
- Boecker, Henning
- Brosseron, Frederic
- Buerger, Katharina
- Catak, Cihan
- Fliessbach, Klaus
- Franke, Christiana
- Fuentes, Manuel
- Heneka, Michael T
- Janowitz, Daniel
- Kilimann, Ingo
- Laske, Christoph
- Menne, Felix
- Nestor, Peter
- Peters, Oliver
- Priller, Josef
- Pross, Verena
- Ramirez, Alfredo
- Schneider, Anja
- Speck, Oliver
- Spruth, Eike Jakob
- Teipel, Stefan
- Vukovich, Ruth
- Westerteicher, Christine
- Wiltfang, Jens
- Wolfsgruber, Steffen
- Wagner, Michael
- Düzel, Emrah
Producer: 20190916
In:
Alzheimer's research & therapy vol. 10
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112.
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A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2. [electronic resource] by
- Karsak, Meliha
- Glebov, Konstantin
- Scheffold, Marina
- Bajaj, Thomas
- Kawalia, Amit
- Karaca, Ilker
- Rading, Sebastian
- Kornhuber, Johannes
- Peters, Oliver
- Diez-Fairen, Monica
- Frölich, Lutz
- Hüll, Michael
- Wiltfang, Jens
- Scherer, Martin
- Riedel-Heller, Steffi
- Schneider, Anja
- Heneka, Michael T
- Fliessbach, Klaus
- Sharaf, Ahmed
- Thiele, Holger
- Lennarz, Martina
- Jessen, Frank
- Maier, Wolfgang
- Kubisch, Christian
- Ignatova, Zoya
- Nürnberg, Peter
- Pastor, Pau
- Walter, Jochen
- Ramirez, Alfredo
Producer: 20210519
In:
Human mutation vol. 41
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113.
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Apolipoprotein E ε4 does not affect cognitive performance in patients with Parkinson's disease. [electronic resource] by
- Mengel, David
- Dams, Judith
- Ziemek, Jannis
- Becker, Julian
- Balzer-Geldsetzer, Monika
- Hilker, Rüdiger
- Baudrexel, Simon
- Kalbe, Elke
- Schmidt, Nele
- Witt, Karsten
- Liepelt-Scarfone, Inga
- Gräber, Susanne
- Petrelli, Annette
- Neuser, Petra
- Schulte, Claudia
- Linse, Katharina
- Storch, Alexander
- Wittchen, Hans-Ulrich
- Riedel, Oliver
- Mollenhauer, Brit
- Ebentheuer, Jens
- Trenkwalder, Claudia
- Klockgether, Thomas
- Spottke, Annika
- Wüllner, Ullrich
- Schulz, Jörg B
- Reetz, Kathrin
- Heber, Ines Ann
- Ramirez, Alfredo
- Dodel, Richard
Producer: 20180205
In:
Parkinsonism & related disorders vol. 29
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114.
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Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairment. [electronic resource] by
- Louwersheimer, Eva
- Wolfsgruber, Steffen
- Espinosa, Ana
- Lacour, André
- Heilmann-Heimbach, Stefanie
- Alegret, Montserrat
- Hernández, Isabel
- Rosende-Roca, Maitée
- Tárraga, Lluís
- Boada, Mercè
- Kornhuber, Johannes
- Peters, Oliver
- Frölich, Lutz
- Hüll, Michael
- Rüther, Eckart
- Wiltfang, Jens
- Scherer, Martin
- Riedel-Heller, Steffi
- Jessen, Frank
- Nöthen, Markus M
- Maier, Wolfgang
- Koene, Ted
- Scheltens, Philip
- Holstege, Henne
- Wagner, Michael
- Ruiz, Agustín
- van der Flier, Wiesje M
- Becker, Tim
- Ramirez, Alfredo
Producer: 20171006
In:
Alzheimer's & dementia : the journal of the Alzheimer's Association vol. 12
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115.
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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene. [electronic resource] by
- Lohmann, Katja
- Wilcox, Robert A
- Winkler, Susen
- Ramirez, Alfredo
- Rakovic, Aleksandar
- Park, Jin-Sung
- Arns, Björn
- Lohnau, Thora
- Groen, Justus
- Kasten, Meike
- Brüggemann, Norbert
- Hagenah, Johann
- Schmidt, Alexander
- Kaiser, Frank J
- Kumar, Kishore R
- Zschiedrich, Katja
- Alvarez-Fischer, Daniel
- Altenmüller, Eckart
- Ferbert, Andreas
- Lang, Anthony E
- Münchau, Alexander
- Kostic, Vladimir
- Simonyan, Kristina
- Agzarian, Marc
- Ozelius, Laurie J
- Langeveld, Antonius P M
- Sue, Carolyn M
- Tijssen, Marina A J
- Klein, Christine
Producer: 20140505
In:
Annals of neurology vol. 73
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116.
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PLD3 in non-familial Alzheimer's disease. [electronic resource] by
- Heilmann, Stefanie
- Drichel, Dmitriy
- Clarimon, Jordi
- Fernández, Victoria
- Lacour, André
- Wagner, Holger
- Thelen, Mathias
- Hernández, Isabel
- Fortea, Juan
- Alegret, Montserrat
- Blesa, Rafael
- Mauleón, Ana
- Roca, Maitée Rosende
- Kornhuber, Johannes
- Peters, Oliver
- Heun, Reinhard
- Frölich, Lutz
- Hüll, Michael
- Heneka, Michael T
- Rüther, Eckart
- Riedel-Heller, Steffi
- Scherer, Martin
- Wiltfang, Jens
- Jessen, Frank
- Becker, Tim
- Tárraga, Lluís
- Boada, Mercè
- Maier, Wolfgang
- Lleó, Alberto
- Ruiz, Agustin
- Nöthen, Markus M
- Ramirez, Alfredo
Producer: 20150430
In:
Nature vol. 520
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117.
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Multicenter Tract-Based Analysis of Microstructural Lesions within the Alzheimer's Disease Spectrum: Association with Amyloid Pathology and Diagnostic Usefulness. [electronic resource] by
- Teipel, Stefan J
- Kuper-Smith, Jan O
- Bartels, Claudia
- Brosseron, Frederic
- Buchmann, Martina
- Buerger, Katharina
- Catak, Cihan
- Janowitz, Daniel
- Dechent, Peter
- Dobisch, Laura
- Ertl-Wagner, Birgit
- Fließbach, Klaus
- Haynes, John-Dylan
- Heneka, Michael T
- Kilimann, Ingo
- Laske, Christoph
- Li, Siyao
- Menne, Felix
- Metzger, Coraline D
- Priller, Josef
- Pross, Verena
- Ramirez, Alfredo
- Scheffler, Klaus
- Schneider, Anja
- Spottke, Annika
- Spruth, Eike J
- Wagner, Michael
- Wiltfang, Jens
- Wolfsgruber, Steffen
- Düzel, Emrah
- Jessen, Frank
- Dyrba, Martin
Producer: 20201117
In:
Journal of Alzheimer's disease : JAD vol. 72
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118.
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Which features of subjective cognitive decline are related to amyloid pathology? Findings from the DELCODE study. [electronic resource] by
- Miebach, Lisa
- Wolfsgruber, Steffen
- Polcher, Alexandra
- Peters, Oliver
- Menne, Felix
- Luther, Katja
- Incesoy, Enise
- Priller, Josef
- Spruth, Eike
- Altenstein, Slawek
- Buerger, Katharina
- Catak, Cihan
- Janowitz, Daniel
- Perneczky, Robert
- Utecht, Julia
- Laske, Christoph
- Buchmann, Martina
- Schneider, Anja
- Fliessbach, Klaus
- Kalbhen, Pascal
- Heneka, Michael T
- Brosseron, Frederic
- Spottke, Annika
- Roy, Nina
- Teipel, Stefan J
- Kilimann, Ingo
- Wiltfang, Jens
- Bartels, Claudia
- Düzel, Emrah
- Dobisch, Laura
- Metzger, Coraline
- Meiberth, Dix
- Ramirez, Alfredo
- Jessen, Frank
- Wagner, Michael
Producer: 20200716
In:
Alzheimer's research & therapy vol. 11
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119.
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Alzheimer's disease-associated (hydroxy)methylomic changes in the brain and blood. [electronic resource] by
- Lardenoije, Roy
- Roubroeks, Janou A Y
- Pishva, Ehsan
- Leber, Markus
- Wagner, Holger
- Iatrou, Artemis
- Smith, Adam R
- Smith, Rebecca G
- Eijssen, Lars M T
- Kleineidam, Luca
- Kawalia, Amit
- Hoffmann, Per
- Luck, Tobias
- Riedel-Heller, Steffi
- Jessen, Frank
- Maier, Wolfgang
- Wagner, Michael
- Hurlemann, René
- Kenis, Gunter
- Ali, Muhammad
- Del Sol, Antonio
- Mastroeni, Diego
- Delvaux, Elaine
- Coleman, Paul D
- Mill, Jonathan
- Rutten, Bart P F
- Lunnon, Katie
- Ramirez, Alfredo
- van den Hove, Daniël L A
Producer: 20200727
In:
Clinical epigenetics vol. 11
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120.
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TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis. [electronic resource] by
- Kleinberger, Gernot
- Yamanishi, Yoshinori
- Suárez-Calvet, Marc
- Czirr, Eva
- Lohmann, Ebba
- Cuyvers, Elise
- Struyfs, Hanne
- Pettkus, Nadine
- Wenninger-Weinzierl, Andrea
- Mazaheri, Fargol
- Tahirovic, Sabina
- Lleó, Alberto
- Alcolea, Daniel
- Fortea, Juan
- Willem, Michael
- Lammich, Sven
- Molinuevo, José L
- Sánchez-Valle, Raquel
- Antonell, Anna
- Ramirez, Alfredo
- Heneka, Michael T
- Sleegers, Kristel
- van der Zee, Julie
- Martin, Jean-Jacques
- Engelborghs, Sebastiaan
- Demirtas-Tatlidede, Asli
- Zetterberg, Henrik
- Van Broeckhoven, Christine
- Gurvit, Hakan
- Wyss-Coray, Tony
- Hardy, John
- Colonna, Marco
- Haass, Christian
Producer: 20150223
In:
Science translational medicine vol. 6
Availability: No items available.
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