|
🐜
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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies.
121 auth.
S. Appenzeller,
R. Balling,
N. Barišić,
S. Baulac,
H. Caglayan,
D. Craiu,
P. Jonghe,
C. Depienne,
P. Dimova,
T. Djémié,
P. Gormley,
R. Guerrini,
I. Helbig,
H. Hjalgrim,
D. Hoffman-Zacharska,
...
J. Jähn,
K. Klein,
B. Koeleman,
V. Komárek,
R. Krause,
G. Kuhlenbäumer,
E. Leguern,
A. Lehesjoki,
J. Lemke,
H. Lerche,
T. Linnankivi,
C. Marini,
P. May,
R. Møller,
H. Muhle,
D. Pal,
A. Palotie,
Manuela Pendziwiat,
A. Robbiano,
F. Roelens,
F. Rosenow,
K. Selmer,
J. Serratosa,
S. Sisodiya,
U. Stephani,
K. Štěrbová,
P. Striano,
A. Suls,
T. Talvik,
S. Spiczak,
Y. Weber,
S. Weckhuysen,
F. Zara,
B. Abou-Khalil,
B. Alldredge,
E. Andermann,
F. Andermann,
D. Amrom,
J. Bautista,
S. Berkovic,
J. Bluvstein,
A. Boro,
G. Cascino,
D. Consalvo,
P. Crumrine,
O. Devinsky,
D. Dlugos,
Michael P. Epstein,
M. Fiol,
N. Fountain,
J. French,
D. Friedman,
Eric B. Geller,
T. Glauser,
Simon Glynn,
K. Haas,
S. Haut,
Jean Hayward,
S. Helmers,
Sucheta M Joshi,
A. Kanner,
Heidi E. Kirsch,
R. C. Knowlton,
E. Kossoff,
R. Kuperman,
R. Kuzniecky,
D. Lowenstein,
Shannon M. McGuire,
P. Motika,
Edward J. Novotny,
R. Ottman,
J. Paolicchi,
J. Parent,
Kristen L. Park,
A. Poduri,
L. Sadleir,
I. Scheffer,
R. Shellhaas,
E. Sherr,
Jerry J. Shih,
Rani K. Singh,
J. Sirven,
Michael C. Smith,
Joseph Sullivan,
L. Thio,
Anu Venkat,
E. P. Vining,
G. V. Allmen,
J. Weisenberg,
P. Widdess-Walsh,
M. Winawer,
Andrew S. Allen,
P. Cossette,
N. Delanty,
Evan E. Eichler,
David K. Goldstein,
Yujun Han,
E. Heinzen,
Michael R. Johnson,
A. G. Marson,
H. Mefford,
Sahar Esmaeeli Nieh,
Terence J. O’Brien,
S. Petrou,
S. Petrovski,
E. Ruzzo
|
8 |
2017 |
8
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|
|
🐜
|
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies
112 auth.
R. Anney,
A. Avbersek,
D. Balding,
L. Baum,
F. Becker,
S. Berkovic,
J. Bradfield,
Lawrence C. Brody,
R. Buono,
C. Catarino,
G. Cavalleri,
S. Cherny,
Krishna Chinthapalli,
Alison J. Coffey,
Alastair Compston,
...
P. Cossette,
G. D. Haan,
P. D. Jonghe,
C. D. Kovel,
N. Delanty,
C. Depondt,
D. Dlugos,
Colin P. Doherty,
Christian E. Elger,
Thomas N. Ferraro,
Martha Feucht,
A. Franke,
Jacqueline A. French,
V. Gaus,
David Goldstein,
Hongsheng Gui,
Youling Guo,
H. Hakonarson,
K. Hallman,
E. Heinzen,
I. Helbig,
H. Hjalgrim,
Michael L. Jackson,
Jennifer Jamnadas-Khoda,
Dieter Janz,
Michael R. Johnson,
R. Kälviäinen,
Anne-Mari Kantanen,
Dalia Kasperavičiūtė,
D. K. Trenité,
B. Koeleman,
Wolfram S Kunz,
Patrick Kwan,
Y. L. Lau,
A. Lehesjoki,
H. Lerche,
C. Leu,
Wolfgang Lieb,
D. Lindhout,
Warren Lo,
D. Lowenstein,
A. Malovini,
A. G. Marson,
Mark Mccormack,
J. M. Mills,
M. Moerzinger,
R. Møller,
A. Molloy,
H. Muhle,
M. Newton,
P. Ng,
M. Nöthen,
P. Nürnberg,
Terence J. O’Brien,
Karen L. Oliver,
A. Palotie,
F. Pangilinan,
K. Pernhorst,
S. Petrovski,
Michael D Privitera,
R. Radtke,
P. Reif,
Felix Rosenow,
Ann-Kathrin Ruppert,
Thomas Sander,
T. Scattergood,
Steven C. Schachter,
Christoph J. Schankin,
I. Scheffer,
Bettina Schmitz,
S. Schoch,
PC Sham,
S. Sisodiya,
D. Smith,
Philip E. M. Smith,
Doug Speed,
Michael R. Sperling,
Michael Steffens,
U. Stephanie,
P. Striano,
H. Stroink,
Rainer Surges,
K. Tan,
GN Thomas,
Marian Todaro,
A. Tostevin,
R. Tozzi,
H. Trucks,
F. Visscher,
S. Spiczak,
N. Walley,
Y. Weber,
Zhi Wei,
C. Whelan,
W. Yang,
F. Zara,
F. Zimprich
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7 |
2014 |
7
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|
|
🐜
|
Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy
74 auth.
Andrew S. Allen,
S. Berkovic,
Bradley P. Coe,
Joseph Cook,
P. Cossette,
N. Delanty,
Dennis Dlugos,
Evan E. Eichler,
Michael P. Epstein,
Tracy Glauser,
David B Goldstein,
E. Heinzen,
Michael R. Johnson,
Nik Krumm,
R. Kuzniecky,
...
Daniel Lowenstein,
A. G. Marson,
H. Mefford,
Ben Nelson,
Sahar Esmaeeli Nieh,
Terence J. O’Brien,
Ruth Ottman,
Steven Petrou,
S. Petrovski,
A. Poduri,
A. Raja,
E. Ruzzo,
I. Scheffer,
Elliott Sherr,
B. Abou-Khalil,
B. Alldredge,
E. Andermann,
F. Andermann,
Dina Amron,
J. Bautista,
Alex Boro,
Gregory D. Cascino,
Damian Consalvo,
P. Crumrine,
Orrin Devinsky,
Miguel Fiol,
N. Fountain,
Jacqueline A. French,
Daniel Friedman,
Eric B. Geller,
Simon Glynn,
S. Haut,
Jean Hayward,
S. Helmers,
Sucheta Joshi,
Andres Kanner,
Heidi E. Kirsch,
R. C. Knowlton,
E. Kossoff,
R. Kuperman,
Shannon M. McGuire,
P. Motika,
Edward J. Novotny,
J. Paolicchi,
Jack M. Parent,
Kristen L Park,
R. Shellhaas,
Jerry J. Shih,
Rani K. Singh,
Joseph Sirven,
Michael C. Smith,
Joseph Sullivan,
L. Thio,
Anu Venkat,
E. P. Vining,
G. V. Von Allmen,
J. Weisenberg,
P. Widdess-Walsh,
M. Winawer
|
6 |
2015 |
6
🐜
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|
🐜
|
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
220 auth.
Lisa-Marie Niestroj,
E. Pérez-Palma,
D. Howrigan,
Yadi Zhou,
F. Cheng,
Elmo Saarentaus,
P. Nürnberg,
R. Stevelink,
M. Daly,
A. Palotie,
Dennis Lal,
Yen-Chen Anne Feng,
D. Howrigan,
L. Abbott,
K. Tashman,
...
Felecia Cerrato,
Dennis Lal,
C. Churchhouse,
Namrata Gupta,
B. Neale,
S. Berkovic,
H. Lerche,
David B Goldstein,
D. Lowenstein,
G. Cavalleri,
P. Cossette,
C. Cotsapas,
P. de Jonghe,
Tracy Dixon-Salazar,
R. Guerrini,
H. Hakonarson,
E. Heinzen,
I. Helbig,
Patrick Kwan,
A. G. Marson,
S. Petrovski,
S. Kamalakaran,
S. Sisodiya,
Randy Stewart,
S. Weckhuysen,
C. Depondt,
D. Dlugos,
I. Scheffer,
P. Striano,
C. Freyer,
Roland Krause,
Patrick May,
Kevin McKenna,
Brigid M. Regan,
S. Bellows,
C. Leu,
C. A. Bennett,
E. Johns,
Alexandra Macdonald,
Hannah Shilling,
R. Burgess,
Dorien Weckhuysen,
M. Bahlo,
Terence J. O’Brien,
Marian Todaro,
Hannah Stamberger,
Danielle M. Andrade,
Tara Sadoway,
Kelly Mo,
H. Krestel,
Sabina Gallati,
S. Papacostas,
I. Kousiappa,
G. Tanteles,
K. Štěrbová,
M. Vlčková,
L. Sedláčková,
P. Laššuthová,
K. Klein,
Felix Rosenow,
P. Reif,
S. Knake,
Wolfram S Kunz,
G. Zsurka,
Christian E. Elger,
Jürgen Bauer,
M. Rademacher,
Manuela Pendziwiat,
H. Muhle,
Annika Rademacher,
A. van Baalen,
S. von Spiczak,
U. Stephani,
Z. Afawi,
Amos D. Korczyn,
Moien Kanaan,
Christina Canavati,
G. Kurlemann,
K. Müller-Schlüter,
G. Kluger,
Martin Häusler,
Ilan Blatt,
J. Lemke,
Ilona Krey,
Y. Weber,
S. Wolking,
F. Becker,
Christian Hengsbach,
S. Rau,
A. Maisch,
Bernhard J. Steinhoff,
Andreas Schulze-Bonhage,
S. Schubert-Bast,
Herbert Schreiber,
Ingo Borggräfe,
C. Schankin,
Thomas Mayer,
Rudolf Korinthenberg,
K. Brockmann,
D. Dennig,
R. Madeleyn,
R. Kälviäinen,
P. Auvinen,
Anni Saarela,
T. Linnankivi,
A. Lehesjoki,
M. I. Rees,
S. Chung,
W. O. Pickrell,
Robert Powell,
Natascha Schneider,
S. Balestrini,
S. Zagaglia,
V. Braatz,
Michael R. Johnson,
P. Auce,
G. Sills,
L. Baum,
P. C. Sham,
S. Cherny,
C. Lui,
N. Barišić,
N. Delanty,
Colin P. Doherty,
Arif Shukralla,
Mark Mccormack,
Hany El-Naggar,
L. Canafoglia,
S. Franceschetti,
B. Castellotti,
T. Granata,
F. Zara,
M. Iacomino,
F. Madia,
M. Vari,
M. Mancardi,
V. Salpietro,
F. Bisulli,
P. Tinuper,
L. Licchetta,
T. Pippucci,
C. Stipa,
L. Muccioli,
R. Minardi,
A. Gambardella,
A. Labate,
G. Annesi,
Lorella Manna,
M. Gagliardi,
E. Parrini,
D. Mei,
A. Vetro,
C. Bianchini,
Martino Montomoli,
Viola Doccini,
C. Marini,
Toshimitsu Suzuki,
Yushi Inoue,
Kazuhiro Yamakawa,
Birutė Tumienė,
R. Mameniskiene,
A. Utkus,
Rūta Praninskienė,
Jurgita Grikiniene,
Rūta Samaitienė,
L. Sadleir,
Chontelle King,
Emily Mountier,
S. Caglayan,
M. Arslan,
Z. Yapıcı,
U. Yiş,
Pınar Topaloğlu,
Bulent Kara,
D. Turkdoğan,
Aslı Gundogdu-Eken,
N. Bebek,
Sibel Uğur-İşeri,
B. Baykan,
Barış Salman,
Garen Haryanyan,
E. Yücesan,
Y. Kesim,
Ç. Özkara,
B. Sheidley,
Catherine Shain,
A. Poduri,
R. Buono,
Thomas N. Ferraro,
Michael R. Sperling,
Warren Lo,
Michael D Privitera,
Jacqueline A. French,
Steven C. Schachter,
R. Kuzniecky,
O. Devinsky,
Manu Hegde,
Pouya Khankhanian,
K. Helbig,
C. Ellis,
Gianfranco Spalletta,
F. Piras,
F. Piras,
T. Gili,
V. Ciullo
|
5 |
2020 |
5
🐜
|
|
🐜
|
Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data
105 auth.
Andrew S. Allen,
S. Berkovic,
Joshua Bridgers,
P. Cossette,
D. Dlugos,
Michael P. Epstein,
T. Glauser,
David B Goldstein,
E. Heinzen,
Yu Jiang,
Michael R. Johnson,
R. Kuzniecky,
D. Lowenstein,
A. G. Marson,
H. Mefford,
...
Terence J. O’Brien,
Ruth Ottman,
Steven Petrou,
S. Petrovski,
A. Poduri,
Z. Ren,
I. Scheffer,
E. Sherr,
Quanli Wang,
Rudi Balling,
N. Barišić,
S. Baulac,
H. Caglayan,
D. Craiu,
P. de Jonghe,
C. Depienne,
R. Guerrini,
I. Helbig,
H. Hjalgrim,
D. Hoffman-Zacharska,
J. Jähn,
K. Klein,
B. Koeleman,
V. Komárek,
Roland Krause,
E. Leguern,
A. Lehesjoki,
J. Lemke,
H. Lerche,
T. Linnankivi,
C. Marini,
P. May,
R. Møller,
H. Muhle,
D. Pal,
A. Palotie,
Felix Rosenow,
K. Selmer,
J. Serratosa,
S. Sisodiya,
U. Stephani,
K. Štěrbová,
P. Striano,
A. Suls,
T. Talvik,
S. von Spiczak,
Y. Weber,
S. Weckhuysen,
F. Zara,
B. Abou-Khalil,
B. Alldredge,
D. Amrom,
E. Andermann,
F. Andermann,
J. Bautista,
J. Bluvstein,
G. Cascino,
Damian Consalvo,
P. Crumrine,
O. Devinsky,
M. Fiol,
N. Fountain,
Jacqueline A. French,
Daniel Friedman,
K. Haas,
S. Haut,
Jean Hayward,
Sucheta Joshi,
Andres Kanner,
Heidi E. Kirsch,
E. Kossoff,
R. Kuperman,
Shannon M. McGuire,
P. Motika,
Edward J. Novotny,
Ruth Ottman,
J. Paolicchi,
Jack M. Parent,
Kristen L Park,
R. Shellhaas,
Joseph Sirven,
Michael C. Smith,
Joseph Sullivan,
L. Thio,
Anu Venkat,
E. P. Vining,
G. V. Von Allmen,
J. Weisenberg,
P. Widdess-Walsh,
M. Winawer
|
2 |
2017 |
2
🐜
|
|
🐜
|
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
336 auth.
Siwei Chen,
B. Abou-Khalil,
Z. Afawi,
Q. Z. Ali,
E. Amadori,
Alison Anderson,
Joseph Anderson,
Danielle M. Andrade,
G. Annesi,
M. Arslan,
P. Auce,
Melanie Bahlo,
Mark D. Baker,
G. Balagura,
Simona Balestrini,
...
E. Banks,
Carmen Barba,
Karen Barboza,
Fabrice Bartolomei,
N. Bass,
L. Baum,
Tobias H. Baumgartner,
B. Baykan,
N. Bebek,
F. Becker,
C. A. Bennett,
A. Beydoun,
C. Bianchini,
F. Bisulli,
D. Blackwood,
Ilan Blatt,
Ingo Borggräfe,
C. Boßelmann,
V. Braatz,
Harrison Brand,
Knut Brockmann,
Russell J Buono,
Robyn M. Busch,
S. Caglayan,
L. Canafoglia,
Christina Canavati,
B. Castellotti,
G. Cavalleri,
Felecia Cerrato,
F. Chassoux,
Christina Cherian,
S. Cherny,
Ching-Lung Cheung,
I. Chou,
S. Chung,
C. Churchhouse,
V. Ciullo,
Peggy O. Clark,
Andrew J. Cole,
M. Cosico,
P. Cossette,
C. Cotsapas,
C. Cusick,
M. Daly,
Lea K. Davis,
P. Jonghe,
N. Delanty,
D. Dennig,
C. Depondt,
Philippe Derambure,
Orrin Devinsky,
L. D. Vito,
Faith Dickerson,
Dennis J. Dlugos,
Viola Doccini,
Colin P. Doherty,
Hany El-Naggar,
Colin A. Ellis,
Leon Epstein,
Meghan Evans,
Annika B. Faucon,
Yen-Chen Anne Feng,
Lisa Ferguson,
Thomas N. Ferraro,
Izabela Ferreira Da Silva,
Lorenzo Ferri,
Martha Feucht,
Madeline C Fields,
Mark Fitzgerald,
B. Fonferko-Shadrach,
Francesco Fortunato,
Silvana Franceschetti,
Jacqueline A. French,
E. Freri,
Jack M Fu,
Stacey B. Gabriel,
M. Gagliardi,
A. Gambardella,
L. Gauthier,
T. Giangregorio,
T. Gili,
Tracy A. Glauser,
Ethan Goldberg,
A. Goldman,
David B Goldstein,
Tiziana Granata,
Riley Grant,
David A. Greenberg,
R. Guerrini,
Aslı Gundogdu-Eken,
Namrata Gupta,
Kevin Haas,
H. Hakonarson,
Garen Haryanyan,
Martin Häusler,
Manu Hegde,
E. Heinzen,
I. Helbig,
Christian Hengsbach,
H. Heyne,
Shinichi Hirose,
Edouard Hirsch,
Chen-Jui Ho,
Olivia Hoeper,
D. Howrigan,
Donald Hucks,
Po-Chen Hung,
M. Iacomino,
Yushi Inoue,
L. M. Inuzuka,
A. Ishii,
L. Jehi,
Michael R. Johnson,
M. Johnstone,
Reetta Kälviäinen,
Moien Kanaan,
Bulent Kara,
S. Kariuki,
J. Kegele,
Y. Kesim,
N. Khoueiry-Zgheib,
Jean Khoury,
Chontelle King,
K. Klein,
G. Kluger,
S. Knake,
Fernando Kok,
Amos D. Korczyn,
Rudolf Korinthenberg,
Andreas Koupparis,
I. Kousiappa,
Roland Krause,
M. Krenn,
H. Krestel,
Ilona Krey,
Wolfram S Kunz,
Gerhard Kurlemann,
R. Kuzniecky,
Patrick Kwan,
Maite La Vega-Talbott,
A. Labate,
Austin Lacey,
Dennis Lal,
P. Laššuthová,
S. Lauxmann,
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J. Lemke,
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Chelsea Lowther,
Laura Lubbers,
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Lúcia I Macedo-Souza,
R. Madeleyn,
F. Madia,
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L. Marcuse,
Paula Marques,
A. G. Marson,
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Patrick May,
Thomas Mayer,
W. McArdle,
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P. McGoldrick,
C. McGraw,
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Andrew McQuillan,
K. Meador,
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J. Millichap,
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B. Mostacci,
L. Muccioli,
H. Muhle,
K. Müller-Schlüter,
I. Najm,
W. Nasreddine,
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Seth Owusu-Agyei,
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A. Palotie,
S. Papacostas,
E. Parrini,
C. Pato,
M. Pato,
Manuela Pendziwiat,
P. Pennell,
S. Petrovski,
W. O. Pickrell,
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Dalila Pinto,
T. Pippucci,
F. Piras,
F. Piras,
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Robert Powell,
Michael D Privitera,
Annika Rademacher,
F. Ragona,
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Andrea Salmon,
Vincenzo Salpietro,
I. Sammarra,
Marcello Scala,
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L. Sedláčková,
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P. C. Sham,
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S. A. Siena,
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M. Solomonson,
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Bernhard J. Steinhoff,
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K. Štěrbová,
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C. Stipa,
P. Striano,
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Mariagrazia Talarico,
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N. Timpson,
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Pınar Topaloğlu,
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Nick Watts,
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P. Widdess-Walsh,
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Steven M. Wolf,
M. Wolff,
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Isaac Wong,
R. von Wrede,
David Wu,
Kazuhiro Yamakawa,
Z. Yapıcı,
U. Yiş,
R. Yolken,
E. Yücesan,
S. Zagaglia,
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F. Zimprich,
Milena Zizovic,
G. Zsurka,
B. Neale,
S. Berkovic
|
2 |
2024 |
2
🐜
|
|
🐜
|
2013 Emerging Science Abstracts
35 auth.
Massimo Pandolfo,
L. Dibbens,
B. Vries,
S. Donatello,
S. Heron,
B. Hodgson,
S. Chintawar,
D. Crompton,
James P. Hughes,
S. Bellows,
K. Klein,
P. Callenbach,
M. Corbett,
Alison Gardner,
Sarah Kivity,
...
Xenia Iona,
Brigid M. Regan,
C. Weller,
Denis Crimmins,
Terence J. O’Brien,
R. Guerrero‐López,
J. Mulley,
François Dubeau,
L. Licchetta,
F. Bisulli,
P. Cossette,
Paul Thomas,
Jozef Gecz,
J. Serratosa,
Oebele F. Brouwer,
F. Andermann,
E. Andermann,
A. Maagdenberg,
S. Berkovic,
I. Scheffer
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1 |
2013 |
1
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|
The role of copy number variants in the genetic architecture of common familial epilepsies
93 auth.
Epi4K Consortium,
MD Heather C. Mefford,
E. A. Fuerte,
John Nguyen,
Michelle Mehaffey,
Arvis Sulovari,
Tianyun Wang,
M. Galey,
Danny E Miller,
Evan E. Eichler,
B. Abou-Khalil,
Z. Afawi,
Andrew S. Allen,
D. Amrom,
Eva Andermann,
...
J. Bautista,
S. Bellows,
S. Berkovic,
J. Bluvstein,
Alex Boro,
R. Burgess,
G. Cascino,
Damian Consalvo,
P. Cossette,
D. Crompton,
P. Crumrine,
Sarah W. Curtis,
N. Delanty,
O. Devinsky,
Dennis Dlugos,
Colin A. Ellis,
Michael P. Epstein,
Miguel Fiol,
N. Fountain,
C. Freyer,
Daniel Friedman,
Eric B. Geller,
Tracy Glauser,
Simon Glynn,
David B Goldstein,
Micheline Gravel,
Kevin Haas,
Rebekah V Harris,
S. Haut,
E. Heinzen,
Sandra Helmers,
Olivia J. Henry,
Sucheta Joshi,
Heidi E. Kirsch,
Sarah Kivity,
R. C. Knowlton,
E. Kossoff,
R. Kuzniecky,
Rebecca Loeb,
D. Lowenstein,
A. G. Marson,
Mark Mccormack,
Shannon M. McGuire,
Kevin McKenna,
P. Motika,
Saul A. Mullen,
Edward J. Novotny,
Terence J. O’Brien,
Karen L. Oliver,
J. Paolicchi,
Jack M. Parent,
Kristen L Park,
Sarah J. Paterson,
W. O. Pickrell,
A. Poduri,
M. I. Rees,
L. Sadleir,
Ingrid E. Scheffer,
R. Shellhaas,
E. Sherr,
Jerry J. Shih,
S. Shinnar,
Rani K. Singh,
Joseph Sirven,
Michael C. Smith,
Philip E. M. Smith,
Michael R. Sperling,
Joseph Sullivan,
Liu Lin,
Thio,
Rhys H. Thomas,
Anu Venkat,
E. P. Vining,
G. V. Allmen,
J. Weisenberg,
P. Widdess-Walsh,
M. Winawer,
G. H. Sergievsky
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2023 |
1
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Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families
48 auth.
Karen L. Oliver,
I. Scheffer,
Colin A. Ellis,
B. Grinton,
Z. Afawi,
D. Amrom,
Eva Andermann,
Jocelyn F. Bautista,
S. Bellows,
J. Bluvstein,
Gregory D Cascino,
S. Chung,
P. Cossette,
Sarah W. Curtis,
N. Delanty,
...
Orrin Devinsky,
Dennis J. Dlugos,
Michael P. Epstein,
C. Freyer,
Micheline Gravel,
Rebekah V Harris,
E. Heinzen,
Olivia J. Henry,
Heidi E. Kirsch,
R. C. Knowlton,
E. Kossoff,
Rebecca Loeb,
D. Lowenstein,
A. G. Marson,
H. Mefford,
P. Motika,
Terence J. O’Brien,
Ruth Ottman,
J. Paolicchi,
S. Petrovski,
W. O. Pickrell,
M. I. Rees,
L. Sadleir,
Jerry J. Shih,
Rani K. Singh,
Michael C. Smith,
Philip E. M. Smith,
Rhys H. Thomas,
J. Weisenberg,
P. Widdess-Walsh,
M. Winawer,
Sam F Berkovic,
M. Bahlo
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1 |
2024 |
1
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