Loading Filters
Showing 1–17 of 17 results
-
Comments and Opinion |
-
Research |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy
- Dheeraj R. Bobbili
- , Dennis Lal
- , Patrick May
- , Eva M. Reinthaler
- , Kamel Jabbari
- , Holger Thiele
- , Michael Nothnagel
- , Wiktor Jurkowski
- , Martha Feucht
- , Peter Nürnberg
- , Holger Lerche
- , Fritz Zimprich
- , Roland Krause
- , Bernd A. Neubauer
- , Eva M. Reinthaler
- , Fritz Zimprich
- , Martha Feucht
- , Hannelore Steinböck
- , Birgit Neophytou
- , Julia Geldner
- , Ursula Gruber-Sedlmayr
- , Edda Haberlandt
- , Gabriel M. Ronen
- , Janine Altmüller
- , Dennis Lal
- , Peter Nürnberg
- , Thomas Sander
- , Holger Thiele
- , Roland Krause
- , Patrick May
- , Rudi Balling
- , Holger Lerche
- & Bernd A. Neubauer
-
Research |
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
- Johannes Lemke, Holger Lerche and colleagues report the identification...
- Steffen Syrbe
- , Ulrike B S Hedrich
- , Erik Riesch
- , Tania Djémié
- , Stephan Müller
- , Rikke S Møller
- , Bridget Maher
- , Laura Hernandez-Hernandez
- , Matthis Synofzik
- , Hande S Caglayan
- , Mutluay Arslan
- , José M Serratosa
- , Michael Nothnagel
- , Patrick May
- , Roland Krause
- , Heidrun Löffler
- , Katja Detert
- , Thomas Dorn
- , Heinrich Vogt
- , Günter Krämer
- , Ludger Schöls
- , Primus E Mullis
- , Tarja Linnankivi
- , Anna-Elina Lehesjoki
- , Katalin Sterbova
- , Dana C Craiu
- , Dorota Hoffman-Zacharska
- , Christian M Korff
- , Yvonne G Weber
- , Maja Steinlin
- , Sabina Gallati
- , Astrid Bertsche
- , Matthias K Bernhard
- , Andreas Merkenschlager
- , Wieland Kiess
- , Rudi Balling
- , Nina Barisic
- , Stéphanie Baulac
- , Hande S Caglayan
- , Dana C Craiu
- , Peter De Jonghe
- , Christel Depienne
- , Padhraig Gormley
- , Renzo Guerrini
- , Ingo Helbig
- , Helle Hjalgrim
- , Dorota Hoffman-Zacharska
- , Johanna Jähn
- , Karl Martin Klein
- , Bobby P C Koeleman
- , Vladimir Komarek
- , Roland Krause
- , Eric LeGuern
- , Anna-Elina Lehesjoki
- , Johannes R Lemke
- , Holger Lerche
- , Carla Marini
- , Patrick May
- , Rikke S Møller
- , Hiltrud Muhle
- , Aarno Palotie
- , Deb Pal
- , Felix Rosenow
- , Kaja Selmer
- , José M Serratosa
- , Sanjay M Sisodiya
- , Ulrich Stephani
- , Katalin Sterbova
- , Pasquale Striano
- , Arvid Suls
- , Tiina Talvik
- , Sarah von Spiczak
- , Yvonne G Weber
- , Sarah Weckhuysen
- , Federico Zara
- , Michael Gonzalez
- , Stephan Züchner
- , Aarno Palotie
- , Arvid Suls
- , Peter De Jonghe
- , Ingo Helbig
- , Saskia Biskup
- , Markus Wolff
- , Snezana Maljevic
- , Rebecca Schüle
- , Sanjay M Sisodiya
- , Sarah Weckhuysen
- , Holger Lerche
- & Johannes R Lemke
-
Research |
-
Research | | Open
-
Amendments and Corrections |
Retraction Note: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
- Karsten Haug
- , Maike Warnstedt
- , Alexi K Alekov
- , Thomas Sander
- , Alfredo Ramírez
- , Barbara Poser
- , Snezana Maljevic
- , Simon Hebeisen
- , Christian Kubisch
- , Johannes Rebstock
- , Steve Horvath
- , Kerstin Hallmann
- , Joern S Dullinger
- , Birgit Rau
- , Fritz Haverkamp
- , Stefan Beyenburg
- , Herbert Schulz
- , Dieter Janz
- , Bernd Giese
- , Gerhard Müller-Newen
- , Peter Propping
- , Christian E Elger
- , Christoph Fahlke
- , Holger Lerche
- & Armin Heils
-
Research |
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
- Ingo Helbig
- , Heather C Mefford
- , Andrew J Sharp
- , Michel Guipponi
- , Marco Fichera
- , Andre Franke
- , Hiltrud Muhle
- , Carolien de Kovel
- , Carl Baker
- , Sarah von Spiczak
- , Katherine L Kron
- , Ines Steinich
- , Ailing A Kleefuß-Lie
- , Costin Leu
- , Verena Gaus
- , Bettina Schmitz
- , Karl M Klein
- , Philipp S Reif
- , Felix Rosenow
- , Yvonne Weber
- , Holger Lerche
- , Fritz Zimprich
- , Lydia Urak
- , Karoline Fuchs
- , Martha Feucht
- , Pierre Genton
- , Pierre Thomas
- , Frank Visscher
- , Gerrit-Jan de Haan
- , Rikke S Møller
- , Helle Hjalgrim
- , Daniela Luciano
- , Michael Wittig
- , Michael Nothnagel
- , Christian E Elger
- , Peter Nürnberg
- , Corrado Romano
- , Alain Malafosse
- , Bobby P C Koeleman
- , Dick Lindhout
- , Ulrich Stephani
- , Stefan Schreiber
- , Evan E Eichler
- & Thomas Sander
-
Correspondence |
CLCN2 variants in idiopathic generalized epilepsy
- Ailing Kleefuß-Lie
- , Waltraut Friedl
- , Sven Cichon
- , Karsten Haug
- , Maike Warnstedt
- , Alexi Alekov
- , Thomas Sander
- , Alfredo Ramirez
- , Barbara Poser
- , Snezana Maljevic
- , Simon Hebeisen
- , Christian Kubisch
- , Johannes Rebstock
- , Steve Horvath
- , Kerstin Hallmann
- , Jörn S Dullinger
- , Birgit Rau
- , Fritz Haverkamp
- , Stefan Beyenburg
- , Herbert Schulz
- , Dieter Janz
- , Bernd Giese
- , Gerhard Müller-Newen
- , Peter Propping
- , Christian E Elger
- , Christoph Fahlke
- & Holger Lerche
-
Research | | Open
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish
- Aleksandra Siekierska
- , Hannah Stamberger
- , Tine Deconinck
- , Stephanie N. Oprescu
- , Michèle Partoens
- , Yifan Zhang
- , Jo Sourbron
- , Elias Adriaenssens
- , Patrick Mullen
- , Patrick Wiencek
- , Katia Hardies
- , Jeong-Soo Lee
- , Hoi-Khoanh Giong
- , Felix Distelmaier
- , Orly Elpeleg
- , Katherine L. Helbig
- , Joseph Hersh
- , Sedat Isikay
- , Elizabeth Jordan
- , Ender Karaca
- , Angela Kecskes
- , James R. Lupski
- , Reka Kovacs-Nagy
- , Patrick May
- , Vinodh Narayanan
- , Manuela Pendziwiat
- , Keri Ramsey
- , Sampathkumar Rangasamy
- , Deepali N. Shinde
- , Ronen Spiegel
- , Vincent Timmerman
- , Sarah von Spiczak
- , Ingo Helbig
- , Chris Balak
- , Newell Belnap
- , Ana Claasen
- , Amanda Courtright
- , Matt de Both
- , Matthew J. Huentelman
- , Marcus Naymik
- , Ryan Richholt
- , Ashley L. Siniard
- , Szabolcs Szelinger
- , David W. Craig
- , Isabelle Schrauwen
- , Zaid Afawi
- , Rudi Balling
- , Stéphanie Baulac
- , Nina Barišić
- , Hande S. Caglayan
- , Dana Craiu
- , Rosa Guerrero-López
- , Renzo Guerrini
- , Helle Hjalgrim
- , Johanna Jähn
- , Karl Martin Klein
- , Eric Leguern
- , Johannes R. Lemke
- , Holger Lerche
- , Carla Marini
- , Rikke S. Møller
- , Hiltrud Muhle
- , Felix Rosenow
- , Jose Serratosa
- , Arvid Suls
- , Ulrich Stephani
- , Katalin Štěrbová
- , Pasquale Striano
- , Federico Zara
- , Sarah Weckhuysen
- , Christopher Francklyn
- , Anthony Antonellis
- , Peter de Witte
- & Peter De Jonghe
-
Research | | Open
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
- Bassel Abou-Khalil
- , Pauls Auce
- , Andreja Avbersek
- , Melanie Bahlo
- , David J. Balding
- , Thomas Bast
- , Larry Baum
- , Albert J. Becker
- , Felicitas Becker
- , Bianca Berghuis
- , Samuel F. Berkovic
- , Katja E. Boysen
- , Jonathan P. Bradfield
- , Lawrence C. Brody
- , Russell J. Buono
- , Ellen Campbell
- , Gregory D. Cascino
- , Claudia B. Catarino
- , Gianpiero L. Cavalleri
- , Stacey S. Cherny
- , Krishna Chinthapalli
- , Alison J. Coffey
- , Alastair Compston
- , Antonietta Coppola
- , Patrick Cossette
- , John J. Craig
- , Gerrit-Jan de Haan
- , Peter De Jonghe
- , Carolien G. F. de Kovel
- , Norman Delanty
- , Chantal Depondt
- , Orrin Devinsky
- , Dennis J. Dlugos
- , Colin P. Doherty
- , Christian E. Elger
- , Johan G. Eriksson
- , Thomas N. Ferraro
- , Martha Feucht
- , Ben Francis
- , Andre Franke
- , Jacqueline A. French
- , Saskia Freytag
- , Verena Gaus
- , Eric B. Geller
- , Christian Gieger
- , Tracy Glauser
- , Simon Glynn
- , David B. Goldstein
- , Hongsheng Gui
- , Youling Guo
- , Kevin F. Haas
- , Hakon Hakonarson
- , Kerstin Hallmann
- , Sheryl Haut
- , Erin L. Heinzen
- , Ingo Helbig
- , Christian Hengsbach
- , Helle Hjalgrim
- , Michele Iacomino
- , Andrés Ingason
- , Jennifer Jamnadas-Khoda
- , Michael R. Johnson
- , Reetta Kälviäinen
- , Anne-Mari Kantanen
- , Dalia Kasperavičiūte
- , Dorothee Kasteleijn-Nolst Trenite
- , Heidi E. Kirsch
- , Robert C. Knowlton
- , Bobby P. C. Koeleman
- , Roland Krause
- , Martin Krenn
- , Wolfram S. Kunz
- , Ruben Kuzniecky
- , Patrick Kwan
- , Dennis Lal
- , Yu-Lung Lau
- , Anna-Elina Lehesjoki
- , Holger Lerche
- , Costin Leu
- , Wolfgang Lieb
- , Dick Lindhout
- , Warren D. Lo
- , Iscia Lopes-Cendes
- , Daniel H. Lowenstein
- , Alberto Malovini
- , Anthony G. Marson
- , Thomas Mayer
- , Mark McCormack
- , James L. Mills
- , Nasir Mirza
- , Martina Moerzinger
- , Rikke S. Møller
- , Anne M. Molloy
- , Hiltrud Muhle
- , Mark Newton
- , Ping-Wing Ng
- , Markus M. Nöthen
- , Peter Nürnberg
- , Terence J. O’Brien
- , Karen L. Oliver
- , Aarno Palotie
- , Faith Pangilinan
- , Sarah Peter
- , Slavé Petrovski
- , Annapurna Poduri
- , Michael Privitera
- , Rodney Radtke
- , Sarah Rau
- , Philipp S. Reif
- , Eva M. Reinthaler
- , Felix Rosenow
- , Josemir W. Sander
- , Thomas Sander
- , Theresa Scattergood
- , Steven C. Schachter
- , Christoph J. Schankin
- , Ingrid E. Scheffer
- , Bettina Schmitz
- , Susanne Schoch
- , Pak C. Sham
- , Jerry J. Shih
- , Graeme J. Sills
- , Sanjay M. Sisodiya
- , Lisa Slattery
- , Alexander Smith
- , David F. Smith
- , Michael C. Smith
- , Philip E. Smith
- , Anja C. M. Sonsma
- , Doug Speed
- , Michael R. Sperling
- , Bernhard J. Steinhoff
- , Ulrich Stephani
- , Remi Stevelink
- , Konstantin Strauch
- , Pasquale Striano
- , Hans Stroink
- , Rainer Surges
- , K. Meng Tan
- , Liu Lin Thio
- , G. Neil Thomas
- , Marian Todaro
- , Rossana Tozzi
- , Maria S. Vari
- , Eileen P. G. Vining
- , Frank Visscher
- , Sarah von Spiczak
- , Nicole M. Walley
- , Yvonne G. Weber
- , Zhi Wei
- , Judith Weisenberg
- , Christopher D. Whelan
- , Peter Widdess-Walsh
- , Markus Wolff
- , Stefan Wolking
- , Wanling Yang
- , Federico Zara
- & Fritz Zimprich
-
Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data
- Andrew S Allen
- , Samuel F Berkovic
- , Joshua Bridgers
- , Patrick Cossette
- , Dennis Dlugos
- , Michael P Epstein
- , Tracy Glauser
- , David B Goldstein
- , Erin L Heinzen
- , Yu Jiang
- , Michael R Johnson
- , Ruben Kuzniecky
- , Daniel H Lowenstein
- , Anthony G Marson
- , Heather C Mefford
- , Terence J O'Brien
- , Ruth Ottman
- , Steven Petrou
- , Slavé Petrovski
- , Annapurna Poduri
- , Zhong Ren
- , Ingrid E Scheffer
- , Elliott Sherr
- , Quanli Wang
- , Rudi Balling
- , Nina Barisic
- , Stéphanie Baulac
- , Hande Caglayan
- , Dana Craiu
- , Peter De Jonghe
- , Christel Depienne
- , Renzo Guerrini
- , Ingo Helbig
- , Helle Hjalgrim
- , Dorota Hoffman-Zacharska
- , Johanna Jähn
- , Karl Martin Klein
- , Bobby Koeleman
- , Vladimir Komarek
- , Roland Krause
- , Eric Leguern
- , Anna-Elina Lehesjoki
- , Johannes R Lemke
- , Holger Lerche
- , Tarja Linnankivi
- , Carla Marini
- , Patrick May
- , Rikke S Møller
- , Hiltrud Muhle
- , Deb Pal
- , Aarno Palotie
- , Felix Rosenow
- , Kaja Selmer
- , Jose M Serratosa
- , Sanjay Sisodiya
- , Ulrich Stephani
- , Katalin Sterbova
- , Pasquale Striano
- , Arvid Suls
- , Tiina Talvik
- , Sarah von Spiczak
- , Yvonne Weber
- , Sarah Weckhuysen
- , Federico Zara
- , Bassel Abou-Khalil
- , Brian K Alldredge
- , Dina Amrom
- , Eva Andermann
- , Frederick Andermann
- , Jocelyn F Bautista
- , Samuel F Berkovic
- , Judith Bluvstein
- , Gregory D Cascino
- , Damian Consalvo
- , Patricia Crumrine
- , Orrin Devinsky
- , Dennis Dlugos
- , Michael P Epstein
- , Miguel E Fiol
- , Nathan B Fountain
- , Jacqueline French
- , Daniel Friedman
- , Tracy Glauser
- , Kevin Haas
- , Sheryl R Haut
- , Jean Hayward
- , Sucheta Joshi
- , Andres Kanner
- , Heidi E Kirsch
- , Eric H Kossoff
- , Rachel Kuperman
- , Ruben Kuzniecky
- , Daniel H Lowenstein
- , Shannon M McGuire
- , Paul V Motika
- , Edward J Novotny
- , Ruth Ottman
- , Juliann M Paolicchi
- , Jack Parent
- , Kristen Park
- , Annapurna Poduri
- , Ingrid E Scheffer
- , Renée A Shellhaas
- , Elliott Sherr
- , Joseph Sirven
- , Michael C Smith
- , Joseph Sullivan
- , Liu Lin Thio
- , Anu Venkat
- , Eileen PG Vining
- , Gretchen K Von Allmen
- , Judith L Weisenberg
- , Peter Widdess-Walsh
- & Melodie R Winawer
-
Research | | Open
-
Research |
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
- Holger Lerche, Camila Esguerra and colleagues...
- Julian Schubert
- , Aleksandra Siekierska
- , Mélanie Langlois
- , Patrick May
- , Clément Huneau
- , Felicitas Becker
- , Hiltrud Muhle
- , Arvid Suls
- , Johannes R Lemke
- , Carolien G F de Kovel
- , Holger Thiele
- , Kathryn Konrad
- , Amit Kawalia
- , Mohammad R Toliat
- , Thomas Sander
- , Franz Rüschendorf
- , Almuth Caliebe
- , Inga Nagel
- , Bernard Kohl
- , Angela Kecskés
- , Maxime Jacmin
- , Katia Hardies
- , Sarah Weckhuysen
- , Erik Riesch
- , Thomas Dorn
- , Eva H Brilstra
- , Stephanie Baulac
- , Rikke S Møller
- , Helle Hjalgrim
- , Bobby P C Koeleman
- , Karin Jurkat-Rott
- , Frank Lehmann-Horn
- , Jared C Roach
- , Gustavo Glusman
- , Leroy Hood
- , David J Galas
- , Benoit Martin
- , Peter A M de Witte
- , Saskia Biskup
- , Peter De Jonghe
- , Ingo Helbig
- , Rudi Balling
- , Peter Nürnberg
- , Alexander D Crawford
- , Camila V Esguerra
- , Yvonne G Weber
- & Holger Lerche
-
Research |
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
- Sarah von Spiczak, Holger Lerche and colleagues identify mutations in...
- Johannes R Lemke
- , Dennis Lal
- , Eva M Reinthaler
- , Isabelle Steiner
- , Michael Nothnagel
- , Michael Alber
- , Kirsten Geider
- , Bodo Laube
- , Michael Schwake
- , Katrin Finsterwalder
- , Andre Franke
- , Markus Schilhabel
- , Johanna A Jähn
- , Hiltrud Muhle
- , Rainer Boor
- , Wim Van Paesschen
- , Roberto Caraballo
- , Natalio Fejerman
- , Sarah Weckhuysen
- , Peter De Jonghe
- , Jan Larsen
- , Rikke S Møller
- , Helle Hjalgrim
- , Laura Addis
- , Shan Tang
- , Elaine Hughes
- , Deb K Pal
- , Kadi Veri
- , Ulvi Vaher
- , Tiina Talvik
- , Petia Dimova
- , Rosa Guerrero López
- , José M Serratosa
- , Tarja Linnankivi
- , Anna-Elina Lehesjoki
- , Susanne Ruf
- , Markus Wolff
- , Sarah Buerki
- , Gabriele Wohlrab
- , Judith Kroell
- , Alexandre N Datta
- , Barbara Fiedler
- , Gerhard Kurlemann
- , Gerhard Kluger
- , Andreas Hahn
- , D Edda Haberlandt
- , Christina Kutzer
- , Jürgen Sperner
- , Felicitas Becker
- , Yvonne G Weber
- , Martha Feucht
- , Hannelore Steinböck
- , Birgit Neophythou
- , Gabriel M Ronen
- , Ursula Gruber-Sedlmayr
- , Julia Geldner
- , Robert J Harvey
- , Per Hoffmann
- , Stefan Herms
- , Janine Altmüller
- , Mohammad R Toliat
- , Holger Thiele
- , Peter Nürnberg
- , Christian Wilhelm
- , Ulrich Stephani
- , Ingo Helbig
- , Holger Lerche
- , Fritz Zimprich
- , Bernd A Neubauer
- , Saskia Biskup
- & Sarah von Spiczak
-
Research |
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
- Mikko Muona
- , Samuel F Berkovic
- , Leanne M Dibbens
- , Karen L Oliver
- , Snezana Maljevic
- , Marta A Bayly
- , Tarja Joensuu
- , Laura Canafoglia
- , Silvana Franceschetti
- , Roberto Michelucci
- , Salla Markkinen
- , Sarah E Heron
- , Michael S Hildebrand
- , Eva Andermann
- , Frederick Andermann
- , Antonio Gambardella
- , Paolo Tinuper
- , Laura Licchetta
- , Ingrid E Scheffer
- , Chiara Criscuolo
- , Alessandro Filla
- , Edoardo Ferlazzo
- , Jamil Ahmad
- , Adeel Ahmad
- , Betul Baykan
- , Edith Said
- , Meral Topcu
- , Patrizia Riguzzi
- , Mary D King
- , Cigdem Ozkara
- , Danielle M Andrade
- , Bernt A Engelsen
- , Arielle Crespel
- , Matthias Lindenau
- , Ebba Lohmann
- , Veronica Saletti
- , João Massano
- , Michael Privitera
- , Alberto J Espay
- , Birgit Kauffmann
- , Michael Duchowny
- , Rikke S Møller
- , Rachel Straussberg
- , Zaid Afawi
- , Bruria Ben-Zeev
- , Kaitlin E Samocha
- , Mark J Daly
- , Steven Petrou
- , Holger Lerche
- , Aarno Palotie
- & Anna-Elina Lehesjoki
-
Research |
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
- Caroline Nava
- , Carine Dalle
- , Agnès Rastetter
- , Pasquale Striano
- , Carolien G F de Kovel
- , Rima Nabbout
- , Claude Cancès
- , Dorothée Ville
- , Eva H Brilstra
- , Giuseppe Gobbi
- , Emmanuel Raffo
- , Delphine Bouteiller
- , Yannick Marie
- , Oriane Trouillard
- , Angela Robbiano
- , Boris Keren
- , Dahbia Agher
- , Emmanuel Roze
- , Suzanne Lesage
- , Aude Nicolas
- , Alexis Brice
- , Michel Baulac
- , Cornelia Vogt
- , Nady El Hajj
- , Eberhard Schneider
- , Arvid Suls
- , Sarah Weckhuysen
- , Padhraig Gormley
- , Anna-Elina Lehesjoki
- , Peter De Jonghe
- , Ingo Helbig
- , Stéphanie Baulac
- , Federico Zara
- , Bobby P C Koeleman
- , Rudi Balling
- , Nina Barisic
- , Stéphanie Baulac
- , Hande S Caglayan
- , Dana C Craiu
- , Peter De Jonghe
- , Christel Depienne
- , Padhraig Gormley
- , Renzo Guerrini
- , Ingo Helbig
- , Helle Hjalgrim
- , Dorota Hoffman-Zacharska
- , Johanna Jähn
- , Karl Martin Klein
- , Bobby P C Koeleman
- , Vladimir Komarek
- , Roland Krause
- , Eric LeGuern
- , Anna-Elina Lehesjoki
- , Johannes R Lemke
- , Holger Lerche
- , Carla Marini
- , Patrick May
- , Rikke S Møller
- , Hiltrud Muhle
- , Aarno Palotie
- , Deb Pal
- , Felix Rosenow
- , Kaja Selmer
- , José M Serratosa
- , Sanjay Sisodiya
- , Ulrich Stephani
- , Katalin Sterbova
- , Pasquale Striano
- , Arvid Suls
- , Tiina Talvik
- , Sarah von Spiczak
- , Yvonne Weber
- , Sarah Weckhuysen
- , Federico Zara
- , Thomas Haaf
- , Eric LeGuern
- & Christel Depienne
-
Research |
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
- Karsten Haug
- , Maike Warnstedt
- , Alexi K. Alekov
- , Thomas Sander
- , Alfredo Ramírez
- , Barbara Poser
- , Snezana Maljevic
- , Simon Hebeisen
- , Christian Kubisch
- , Johannes Rebstock
- , Steve Horvath
- , Kerstin Hallmann
- , Joern S. Dullinger
- , Birgit Rau
- , Fritz Haverkamp
- , Stefan Beyenburg
- , Herbert Schulz
- , Dieter Janz
- , Bernd Giese
- , Gerhard Müller-Newen
- , Peter Propping
- , Christian E. Elger
- , Christoph Fahlke
- , Holger Lerche
- & Armin Heils
