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Wyszukujesz frazę ""Racine, Caroline"" wg kryterium: Autor


Tytuł:
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3
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
Chinn, Ivan
Clark, Gary D.
Coakley, Terra R.
Cobban, Laurel A.
Cogan, Joy D.
Coggins, Matthew
Cole, F. Sessions
Colley, Heather A.
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, Audrey Stephannie
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
Seto, Elaine
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.
Tarakad, Arjun
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
Paul, Maimuna S.
Michener, Sydney L.
Pan, Hongling
Chan, Hiuling
Pfliger, Jessica M.
Lerma, Vanesa C.
Tran, Alyssa
Longley, Megan A.
Weisz-Hubshman, Monika
Bekheirnia, Mir Reza
Bekheirnia, Nasim
Massingham, Lauren
Zech, Michael
Wagner, Matias
Engels, Hartmut
Cremer, Kirsten
Mangold, Elisabeth
Peters, Sophia
Trautmann, Jessica
Perne, Claudia
Mester, Jessica L.
Guillen Sacoto, Maria J.
Person, Richard
McDonnell, Pamela P.
Cohen, Stacey R.
Lusk, Laina
Cohen, Ana S.A.
Le Pichon, Jean-Baptiste
Pastinen, Tomi
Zhou, Dihong
Engleman, Kendra
Racine, Caroline
Faivre, Laurence
Moutton, Sébastien
Denommé-Pichon, Anne-Sophie
Koh, Hyun Yong
Poduri, Annapurna
Bolton, Jeffrey
Knopp, Cordula
Julia Suh, Dong Sun
Maier, Andrea
Toosi, Mehran Beiraghi
Karimiani, Ehsan Ghayoor
Maroofian, Reza
Schaefer, Gerald Bradley
Ramakumaran, Vijayalakshmi
Vasudevan, Pradeep
Banos-Pinero, Benito
Pagnamenta, Alistair T.
Prasad, Chitra
Osmond, Matthew
Schuhmann, Sarah
Vasileiou, Georgia
Russ-Hall, Sophie
Scheffer, Ingrid E.
Carvill, Gemma L.
Pokaż więcej
Źródło:
In The American Journal of Human Genetics 4 January 2024 111(1):96-118
Czasopismo naukowe
Tytuł:
Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders
Autorzy:
Tran Mau-Them, FredericAff1, Aff2
Moutton, SebastienAff1, Aff3
Racine, Caroline
Vitobello, AntonioAff1, Aff2
Bruel, Ange-LineAff1, Aff2
Nambot, SophieAff1, Aff3
Kushner, Steven A.
de Vrij, Femke M. S.
Lehalle, DaphnéAff1, Aff3
Jean-Marçais, Nolwenn
Lecoquierre, François
Delanne, Julian
Thevenon, Julien
Poe, Charlotte
Jouan, Thibaut
Chevarin, Martin
Geneviève, DavidAff5, Aff6
Willems, Marjolaine
Coubes, Christine
Houcinat, NadaAff1, Aff3
Masurel-Paulet, Alice
Mosca-Boidron, Anne-LaureAff1, Aff2
Tisserant, Emilie
Callier, PatrickAff1, Aff2
Sorlin, ArthurAff1, Aff2, Aff3
Duffourd, Yannis
Faivre, LaurenceAff1, Aff3
Philippe, ChristopheAff1, Aff2
Thauvin-Robinet, ChristelAff1, Aff2, Aff3, Aff7
Pokaż więcej
Źródło:
Human Genetics. 139(11):1381-1390
Czasopismo naukowe
Tytuł:
A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis
Autorzy:
Arnaud, PaulineAff1, Aff2, Aff3
Racine, Caroline
Hanna, NadineAff1, Aff2
Thevenon, Julien
Alessandri, Jean-Luc
Bonneau, Dominique
Clayton-Smith, JillAff8, Aff9
Coubes, Christine
Delobel, Bruno
Dupuis-Girod, Sophie
Gouya, Laurent
Odent, Sylvie
Carmignac, VirginieAff15, Aff16
Thauvin-Robinet, ChristelAff15, Aff16, Aff17
Le Goff, Carine
Jondeau, GuillaumeAff1, Aff13
Boileau, CatherineAff1, Aff2, Aff3
Faivre, LaurenceAff4, Aff15, Aff16
Pokaż więcej
Źródło:
Human Genetics. 139(4):461-472
Czasopismo naukowe
Tytuł:
The Development of the Obsessive-Compulsive Disorder School Impact Scale: An Investigation Using the Accuracy-Reliability Paradigm for Scale Validation.
Autorzy:
Kratochwill, Thomas R.
Johnston, Hugh
Racine, Caroline N.
Wisconsin Center for Education Research, Madison.
Pokaż więcej
Deskryptory:
Behavior Disorders
Behavior Patterns
Behavior Rating Scales
Elementary Secondary Education
Emotional Disturbances
Psychometrics
Test Construction
Test Reliability
Test Validity
Recenzowane naukowo:
N
Page Count:
205
Sponsoring Agency:
Office of Special Education and Rehabilitative Services (ED), Washington, DC.
Raport
Tytuł:
10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France.
Autorzy:
Messiaen, Claude (AUTHOR)
Racine, Caroline (AUTHOR)
Khatim, Ahlem (AUTHOR)
Soussand, Louis (AUTHOR)
Odent, Sylvie (AUTHOR)
Lacombe, Didier (AUTHOR)
Manouvrier, Sylvie (AUTHOR)
Edery, Patrick (AUTHOR)
Sigaudy, Sabine (AUTHOR)
Geneviève, David (AUTHOR)
Thauvin-Robinet, Christel (AUTHOR)
Pasquier, Laurent (AUTHOR)
Petit, Florence (AUTHOR)
Rossi, Massimiliano (AUTHOR)
Willems, Marjolaine (AUTHOR)
Attié-Bitach, Tania (AUTHOR)
Roux-Levy, Pierre-Henry (AUTHOR)
Demougeot, Laurent (AUTHOR)
Slama, Lilia Ben (AUTHOR)
Landais, Paul (AUTHOR)
Pokaż więcej
Źródło:
Orphanet Journal of Rare Diseases. 8/4/2021, Vol. 16 Issue 1, p1-14. 14p.
Czasopismo naukowe

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