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Search Results - Bridgers, Samuel L.
Search Results - Bridgers, Samuel L.
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Silent cerebral infarction in patients with nonrheumatic atrial fibrillation
by
EZEKOWITZ, M. D
,
JAMES, K. E
,
NAZARIAN, S. M
,
DAVENPORT, J
,
BRODERICK, J. P
,
GUPTA, S. R
,
VIJAY THADANI
,
MEYER, M. L
,
BRIDGERS, S. L
Published in
Circulation (New York, N.Y.)
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Neuropsychological signs of asymptomatic carotid stenosis
by
Naugle, Richard I.
,
Bridgers, Samuel L.
,
Delaney, Richard C.
Published in
Archives of clinical neuropsychology
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Neuropsychological signs of asymptomatic carotid stenosis
by
Naugle, Richard I.
,
Bridgers, Samuel L.
,
Delaney, Richard C.
Published in
Archives of clinical neuropsychology
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A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations
by
Zhu, Xiaolin
,
Padmanabhan, Raghavendra
,
Copeland, Brett
,
Bridgers, Joshua
,
Ren, Zhong
,
Kamalakaran, Sitharthan
,
O'Driscoll-Collins, Ailbhe
,
Berkovic, Samuel F
,
Scheffer, Ingrid E
,
Poduri, Annapurna
,
Mei, Davide
,
Guerrini, Renzo
,
Lowenstein, Daniel H
,
Allen, Andrew S
,
Heinzen, Erin L
,
Goldstein, David B
Published in
PLoS genetics
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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
by
Allen, Andrew S
,
Bellows, Susannah T
,
Berkovic, Samuel F
,
Bridgers, Joshua
,
Burgess, Rosemary
,
Cavalleri, Gianpiero
,
Chung, Seo-Kyung
,
Cossette, Patrick
,
Delanty, Norman
,
Dlugos, Dennis
,
Epstein, Michael P
,
Freyer, Catharine
,
Goldstein, David B
,
Heinzen, Erin L
,
Hildebrand, Michael S
,
Johnson, Michael R
,
Kuzniecky, Ruben
,
Lowenstein, Daniel H
,
Marson, Anthony G
,
Mayeux, Richard
,
Mebane, Caroline
,
Mefford, Heather C
,
O'Brien, Terence J
,
Ottman, Ruth
,
Petrou, Steven
,
Petrovski, Slavgé
,
Pickrell, William O
,
Poduri, Annapurna
,
Radtke, Rodney A
,
Rees, Mark I
,
Regan, Brigid M
,
Ren, Zhong
,
Scheffer, Ingrid E
,
Sills, Graeme J
,
Thomas, Rhys H
,
Wang, Quanli
,
Abou-Khalil, Bassel
,
Alldredge, Brian K
,
Amrom, Dina
,
Andermann, Eva
,
Andermann, Frederick
,
Bautista, Jocelyn F.
,
Bluvstein, Judith
,
Boro, Alex
,
Cascino, Gregory D
,
Consalvo, Damian
,
Crumrine, Patricia
,
Devinsky, Orrin
,
Fiol, Miguel
,
Fountain, Nathan B
,
French, Jacqueline
,
Friedman, Daniel
,
Geller, Eric B
,
Glauser, Tracy
,
Glynn, Simon
,
Haas, Kevin
,
Haut, Sheryl R
,
Hayward, Jean
,
Helmers, Sandra L
,
Joshi, Sucheta
,
Kanner, Andres
,
Kirsch, Heidi E
,
Knowlton, Robert C
,
Kossoff, Eric H
,
Kuperman, Rachel
,
Motika, Paul V
,
Novotny, Edward J
,
Paolicchi, Juliann M
,
Parent, Jack M
,
Park, Kristen
,
Sadleir, Lynette G
,
Shellhaas, Renée A.
,
Sherr, Elliott H
,
Shih, Jerry J.
,
Shinnar, Shlomo
,
Singh, Rani K
,
Sirven, Joseph
,
Smith, Michael C
,
Sullivan, Joseph
,
Thio, Liu Lin
,
Venkat, Anu
,
Vining, Eileen P.G
,
Von Allmen, Gretchen K
,
Weisenberg, Judith L
,
Widdess-Walsh, Peter
,
Winawer, Melodie R
Published in
Lancet neurology
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Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data
by
Allen, Andrew S
,
Berkovic, Samuel F
,
Bridgers, Joshua
,
Cossette, Patrick
,
Dlugos, Dennis
,
Epstein, Michael P
,
Glauser, Tracy
,
Goldstein, David B
,
Heinzen, Erin L
,
Jiang, Yu
,
Johnson, Michael R
,
Kuzniecky, Ruben
,
Lowenstein, Daniel H
,
Marson, Anthony G
,
Mefford, Heather C
,
O'Brien, Terence J
,
Ottman, Ruth
,
Petrou, Steven
,
Petrovski, Slave
,
Poduri, Annapurna
,
Ren, Zhong
,
Scheffer, Ingrid E
,
Sherr, Elliott
,
Wang, Quanli
,
Balling, Rudi
,
Barisic, Nina
,
Baulac, Stephanie
,
Caglayan, Hande
,
Craiu, Dana
,
De Jonghe, Peter
,
Depienne, Christel
,
Guerrini, Renzo
,
Helbig, Ingo
,
Hjalgrim, Helle
,
Hoffman-Zacharska, Dorota
,
Jaehn, Johanna
,
Klein, Karl Martin
,
Koeleman, Bobby
,
Komarek, Vladimir
,
Krause, Roland
,
Leguern, Eric
,
Lehesjoki, Anna-Elina
,
Lemke, Johannes R
,
Lerche, Holger
,
Linnankivi, Tarja
,
Marini, Carla
,
May, Patrick
,
Moeller, Rikke S
,
Muhle, Hiltrud
,
Pal, Deb
,
et. al
Published in
European journal of human genetics : EJHG
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