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Wyszukujesz frazę ""van der Smagt, Jasper"" wg kryterium: Autor


Tytuł:
De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling
Autorzy:
Acosta, Maria T.
Adam, Margaret
Adams, David R.
Alvarez, Raquel L.
Alvey, Justin
Amendola, Laura
Andrews, Ashley
Ashley, Euan A.
Bacino, Carlos A.
Bademci, Guney
Balasubramanyam, Ashok
Baldridge, Dustin
Bale, Jim
Bamshad, Michael
Barbouth, Deborah
Bayrak-Toydemir, Pinar
Beck, Anita
Beggs, Alan H.
Behrens, Edward
Bejerano, Gill
Bellen, Hugo J.
Bennett, Jimmy
Berg-Rood, Beverly
Bernstein, Jonathan A.
Berry, Gerard T.
Bican, Anna
Bivona, Stephanie
Blue, Elizabeth
Bohnsack, John
Bonner, Devon
Botto, Lorenzo
Boyd, Brenna
Briere, Lauren C.
Brown, Gabrielle
Burke, Elizabeth A.
Burrage, Lindsay C.
Butte, Manish J.
Byers, Peter
Byrd, William E.
Carey, John
Carrasquillo, Olveen
Cassini, Thomas
Chang, Ta Chen Peter
Chanprasert, Sirisak
Chao, Hsiao-Tuan
Clark, Gary D.
Coakley, Terra R.
Cobban, Laurel A.
Cogan, Joy D.
Coggins, Matthew
Cole, F. Sessions
Colley, Heather A.
Cooper, Cynthia M.
Cope, Heidi
Corona, Rosario
Craigen, William J.
Crouse, Andrew B.
Cunningham, Michael
D’Souza, Precilla
Dai, Hongzheng
Dasari, Surendra
Davis, Joie
Dayal, Jyoti G.
Dell'Angelica, Esteban C.
Dipple, Katrina
Doherty, Daniel
Dorrani, Naghmeh
Doss, Argenia L.
Douine, Emilie D.
Earl, Dawn
Eckstein, David J.
Emrick, Lisa T.
Eng, Christine M.
Falk, Marni
Fieg, Elizabeth L.
Fisher, Paul G.
Fogel, Brent L.
Forghani, Irman
Gahl, William A.
Glass, Ian
Gochuico, Bernadette
Goddard, Page C.
Godfrey, Rena A.
Golden-Grant, Katie
Grajewski, Alana
Hadley, Don
Hahn, Sihoun
Halley, Meghan C.
Hamid, Rizwan
Hassey, Kelly
Hayes, Nichole
High, Frances
Hing, Anne
Hisama, Fuki M.
Holm, Ingrid A.
Hom, Jason
Horike-Pyne, Martha
Huang, Alden
Hutchison, Sarah
Introne, Wendy
Isasi, Rosario
Izumi, Kosuke
Jamal, Fariha
Jarvik, Gail P.
Jarvik, Jeffrey
Jayadev, Suman
Jean-Marie, Orpa
Jobanputra, Vaidehi
Karaviti, Lefkothea
Ketkar, Shamika
Kiley, Dana
Kilich, Gonench
Kobren, Shilpa N.
Kohane, Isaac S.
Kohler, Jennefer N.
Korrick, Susan
Kozuira, Mary
Krakow, Deborah
Krasnewich, Donna M.
Kravets, Elijah
Lalani, Seema R.
Lam, Byron
Lam, Christina
Lanpher, Brendan C.
Lanza, Ian R.
LeBlanc, Kimberly
Lee, Brendan H.
Levitt, Roy
Lewis, Richard A.
Liu, Pengfei
Liu, Xue Zhong
Longo, Nicola
Loo, Sandra K.
Loscalzo, Joseph
Maas, Richard L.
Macnamara, Ellen F.
MacRae, Calum A.
Maduro, Valerie V.
Maghiro, AudreyStephannie
Mahoney, Rachel
Malicdan, May Christine V.
Mamounas, Laura A.
Manolio, Teri A.
Mao, Rong
Maravilla, Kenneth
Marom, Ronit
Marth, Gabor
Martin, Beth A.
Martin, Martin G.
Martínez-Agosto, Julian A.
Marwaha, Shruti
McCauley, Jacob
McConkie-Rosell, Allyn
McCray, Alexa T.
McGee, Elisabeth
Mefford, Heather
Merritt, J. Lawrence
Might, Matthew
Mirzaa, Ghayda
Morava, Eva
Moretti, Paolo
Mulvihill, John
Nakano-Okuno, Mariko
Nelson, Stanley F.
Newman, John H.
Nicholas, Sarah K.
Nickerson, Deborah
Nieves-Rodriguez, Shirley
Novacic, Donna
Oglesbee, Devin
Orengo, James P.
Pace, Laura
Pak, Stephen
Pallais, J. Carl
Palmer, Christina G.S.
Papp, Jeanette C.
Parker, Neil H.
Phillips III, John A.
Posey, Jennifer E.
Potocki, Lorraine
Pusey Swerdzewski, Barbara N.
Quinlan, Aaron
Rao, Deepak A.
Raper, Anna
Raskind, Wendy
Renteria, Genecee
Reuter, Chloe M.
Rives, Lynette
Robertson, Amy K.
Rodan, Lance H.
Rosenfeld, Jill A.
Rosenwasser, Natalie
Rossignol, Francis
Ruzhnikov, Maura
Sacco, Ralph
Sampson, Jacinda B.
Saporta, Mario
Schaechter, Judy
Schedl, Timothy
Schoch, Kelly
Scott, Daryl A.
Scott, C. Ron
Shashi, Vandana
Shin, Jimann
Silverman, Edwin K.
Sinsheimer, Janet S.
Sisco, Kathy
Smith, Edward C.
Smith, Kevin S.
Solnica-Krezel, Lilianna
Solomon, Ben
Spillmann, Rebecca C.
Stoler, Joan M.
Sullivan, Kathleen
Sullivan, Jennifer A.
Sun, Angela
Sutton, Shirley
Sweetser, David A.
Sybert, Virginia
Tabor, Holly K.
Tan, Queenie K.-G.
Tan, Amelia L.M.
Tekin, Mustafa
Telischi, Fred
Thorson, Willa
Tifft, Cynthia J.
Toro, Camilo
Tran, Alyssa A.
Ungar, Rachel A.
Urv, Tiina K.
Vanderver, Adeline
Velinder, Matt
Viskochil, Dave
Vogel, Tiphanie P.
Wahl, Colleen E.
Walker, Melissa
Wallace, Stephanie
Walley, Nicole M.
Wambach, Jennifer
Wan, Jijun
Wang, Lee-kai
Wangler, Michael F.
Ward, Patricia A.
Wegner, Daniel
Weisz Hubshman, Monika
Wener, Mark
Wenger, Tara
Westerfield, Monte
Wheeler, Matthew T.
Whitlock, Jordan
Wolfe, Lynne A.
Worley, Kim
Xiao, Changrui
Yamamoto, Shinya
Yang, John
Zhang, Zhe
Zuchner, Stephan
Nigro, Vincenzo
Torella, Annalaura
Morleo, Manuela
Spampanato, Carmine
Pinelli, Michele
Banfi, Sandro
Varavallo, Alessandra
Selicorni, Angelo
Mariani, Milena
Massimello, Marta
Daolio, Cecilia
Capra, Valeria
Accogli, Andrea
Scala, Marcello
Leuzzi, Vincenzo
Nardecchia, Francesca
Galosi, Serena
Mastrangelo, Mario
Milani, Donatella
Vitiello, Giuseppina
Piluso, Giulio
Romano, Corrado
Failla, Pinella
Greco, Donatella
Pantaleoni, Chiara
Ciaccio, Claudia
D’Arrigo, Stefano
Brunetti Pierri, Nicola
Parenti, Giancarlo
Coppola, Antonietta
Mattina, Teresa
Zollino, Marcella
Amenta, Simona
Tummolo, Albina
Santoro, Claudia
Grandone, Anna
De Brasi, Daniele
Varone, Antonio
Garavelli, Livia
Marini, Carla
Bigoni, Stefania
Piscopo, Carmelo
Trabacca, Antonio
De Rinaldis, Marta
Peron, Angela
Venditti, Rossella
Theodorou, Evangelos
Rosello, Marion
Tirozzi, Alfonsina
Tammaro, Roberta
Al-Badri, Nour
High, Frances A.
Shi, Jiahai
Putti, Elena
Ferrante, Luigi
Cetrangolo, Viviana
Walker, Melissa A.
Tenconi, Romano
Iascone, Maria
Mei, Davide
Guerrini, Renzo
van der Smagt, Jasper
Kroes, Hester Y.
van Gassen, Koen L.I.
Bilal, Muhammad
Umair, Muhammad
Pingault, Veronica
Attie-Bitach, Tania
Amiel, Jeannine
Ejaz, Resham
Rodan, Lance
Agrawal, Pankaj B.
Del Bene, Filippo
Franco, Brunella
Pokaż więcej
Źródło:
In The American Journal of Human Genetics 3 August 2023 110(8):1377-1393
Czasopismo naukowe
Tytuł:
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration
Autorzy:
Pochiero, Francesca
Mari, Francesco
Ramesh, Venkateswaran
Capra, Valeria
Mancardi, Margherita
Keren, Boris
Mignot, Cyiril
Lulli, Matteo
Parks, Kendall
Griffin, Helen
Brugger, Melanie
Nigro, Vincenzo
Hirata, Yuko
Koichihara, Reiko
Peterlin, Borut
Maki, Ryuto
Nitta, Yohei
Ambrose, John C.
Arumugam, Prabhu
Bevers, Roel
Bleda, Marta
Boardman-Pretty, Freya
Boustred, Christopher R.
Brittain, Helen
Brown, Matthew A.
Caulfield, Mark J.
Chan, Georgia C.
Giess, Adam
Griffin, John N.
Hamblin, Angela
Henderson, Shirley
Hubbard, Tim J.P.
Jackson, Rob
Jones, Louise J.
Kasperaviciute, Dalia
Kayikci, Melis
Kousathanas, Athanasios
Lahnstein, Lea
Lakey, Anna
Leigh, Sarah E.A.
Leong, Ivonne U.S.
Lopez, Javier F.
Maleady-Crowe, Fiona
McEntagart, Meriel
Minneci, Federico
Mitchell, Jonathan
Moutsianas, Loukas
Mueller, Michael
Murugaesu, Nirupa
Need, Anna C.
O’Donovan, Peter
Odhams, Chris A.
Patch, Christine
Perez-Gil, Daniel
Pereira, Marina B.
Pullinger, John
Rahim, Tahrima
Rendon, Augusto
Rogers, Tim
Savage, Kevin
Sawant, Kushmita
Scott, Richard H.
Siddiq, Afshan
Sieghart, Alexander
Smith, Samuel C.
Sosinsky, Alona
Stuckey, Alexander
Tanguy, Mélanie
Taylor Tavares, Ana Lisa
Thomas, Ellen R.A.
Thompson, Simon R.
Tucci, Arianna
Welland, Matthew J.
Williams, Eleanor
Witkowska, Katarzyna
Wood, Suzanne M.
Zarowiecki, Magdalena
Vetro, Annalisa
Pelorosso, Cristiana
Balestrini, Simona
Masi, Alessio
Hambleton, Sophie
Argilli, Emanuela
Conti, Valerio
Giubbolini, Simone
Barrick, Rebekah
Bergant, Gaber
Writzl, Karin
Bijlsma, Emilia K.
Brunet, Theresa
Cacheiro, Pilar
Mei, Davide
Devlin, Anita
Hoffer, Mariëtte J.V.
Machol, Keren
Mannaioni, Guido
Sakamoto, Masamune
Menezes, Manoj P.
Courtin, Thomas
Sherr, Elliott
Parra, Riccardo
Richardson, Ruth
Roscioli, Tony
Scala, Marcello
von Stülpnagel, Celina
Smedley, Damian
Torella, Annalaura
Tohyama, Jun
Hamada, Keisuke
Ogata, Kazuhiro
Suzuki, Takashi
Sugie, Atsushi
van der Smagt, Jasper J.
van Gassen, Koen
Valence, Stephanie
Vittery, Emma
Malone, Stephen
Kato, Mitsuhiro
Matsumoto, Naomichi
Ratto, Gian Michele
Guerrini, Renzo
Pokaż więcej
Źródło:
In The American Journal of Human Genetics 3 August 2023 110(8):1356-1376
Czasopismo naukowe
Tytuł:
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss‐of‐function variants.
Autorzy:
Sewani, Soha
Azamian, Mahshid S.
Mendelsohn, Bryce A.
Mau‐Them, Frederic Tran
Réda, Manon
Nambot, Sophie
Isidor, Bertrand
van der Smagt, Jasper J.
Shen, Joseph J.
Shillington, Amelle
White, Lori
Elloumi, Houda Zghal
Baker, Peter R.
Svihovec, Shayna
Brown, Kathleen
Koopman‐Keemink, Yvonne
Hoffer, Mariette J. V.
Lakeman, Inge M. M.
Brischoux‐Boucher, Elise
Kinali, Maria
Pokaż więcej
Źródło:
American Journal of Medical Genetics. Part A; Mar2024, Vol. 194 Issue 3, p1-12, 12p
Czasopismo naukowe
Tytuł:
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
Autorzy:
Bakshi, Madhura
Wilson, Meredith
Berman, Yemina
Dickson, Rebecca
Fransen, Erik
Helsmoortel, Céline
Van den Ende, Jenneke
Van der Aa, Nathalie
van de Wijdeven, Marina J.
Rosenblum, Jessica
Monteiro, Fabíola
Kok, Fernando
Quercia, Nada
Bowdin, Sarah
Dyment, David
Chitayat, David
Alkhunaizi, Ebba
Boonen, Susanne E.
Keren, Boris
Jacquette, Aurelia
Faivre, Laurence
Bezieau, Stephane
Isidor, Bertrand
Rieß, Angelika
Moog, Ute
Lynch, Sally Ann
McVeigh, Terri
Elpeleg, Orly
Smeland, Marie Falkenberg
Fannemel, Madeleine
van Haeringen, Arie
Maas, Saskia M.
Veenstra-Knol, H.E.
Schouten, Meyke
Willemsen, Marjolein H.
Marcelis, Carlo L.
Ockeloen, Charlotte
van der Burgt, Ineke
Feenstra, Ilse
van der Smagt, Jasper
Jezela-Stanek, Aleksandra
Krajewska-Walasek, Malgorzata
González-Lamuño, Domingo
Anderlid, Britt-Marie
Malmgren, Helena
Nordenskjöld, Magnus
Clement, Emma
Hurst, Jane
Metcalfe, Kay
Mansour, Sahar
Lachlan, Katherine
Clayton-Smith, Jill
Hendon, Laura G.
Abdulrahman, Omar A.
Morrow, Eric
McMillan, Clare
Gerdts, Jennifer
Peeden, Joseph
Schrier Vergano, Samantha A.
Valentino, Caitlin
Chung, Wendy K.
Ozmore, Jillian R.
Bedrosian-Sermone, Sandra
Dennis, Anna
Treat, Kayla
Hughes, Susan Starling
Safina, Nicole
Le Pichon, Jean-Baptiste
McGuire, Marianne
Infante, Elena
Madan-Khetarpal, Suneeta
Desai, Sonal
Benke, Paul
Krokosky, Alyson
Cristian, Ingrid
Baker, Laura
Gripp, Karen
Stessman, Holly A.
Eichenberger, Jacob
Jayakar, Parul
Pizzino, Amy
Manning, Melanie Ann
Slattery, Leah
Van Dijck, Anke
Vulto-van Silfhout, Anneke T.
Cappuyns, Elisa
van der Werf, Ilse M.
Mancini, Grazia M.
Tzschach, Andreas
Bernier, Raphael
Gozes, Illana
Eichler, Evan E.
Romano, Corrado
Lindstrand, Anna
Nordgren, Ann
Kvarnung, Malin
Kleefstra, Tjitske
de Vries, Bert B.A.
Küry, Sébastien
Rosenfeld, Jill A.
Meuwissen, Marije E.
Vandeweyer, Geert
Kooy, R. Frank
Pokaż więcej
Źródło:
In Biological Psychiatry 15 February 2019 85(4):287-297
Czasopismo naukowe
Tytuł:
Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene
Autorzy:
Caliebe, Almuth
Kroes, Hester Y.
van der Smagt, Jasper J.
Martin-Subero, José I.
Tönnies, Holger
van ’t Slot, Ruben
Nievelstein, Rutger A.J.
Muhle, Hiltrud
Stephani, Ulrich
Alfke, Karsten
Stefanova, Irina
Hellenbroich, Yorck
Gillessen-Kaesbach, Gabriele
Hochstenbach, Ron
Siebert, Reiner
Poot, Martin
Pokaż więcej
Źródło:
In European Journal of Medical Genetics 2010 53(4):179-185
Czasopismo naukowe

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