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PLoS genetics, 2021-11, Vol.17 (11), p.e1009854-e1009854
2021
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PLoS genetics, 2019-05, Vol.15 (5), p.e1008143
2019
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PloS one, 2016-03, Vol.11 (3), p.e0151429-e0151429
2016
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Hypertension (Dallas, Tex. 1979), 2022-01, Vol.79 (1), p.60-75
2022
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BMC medical genetics, 2011-03, Vol.12 (1), p.46-46, Article 46
2011
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Orphanet journal of rare diseases, 2015-03, Vol.10 (1), p.27-27, Article 27
2015
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BMC medical genomics, 2016-08, Vol.9 (1), p.56-56, Article 56
2016
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Epilepsia (Copenhagen), 2019-03, Vol.60 (3), p.406-418
- Kelly, McKenna
- Park, Meredith
- Mihalek, Ivana
- Pérez‐Palma, Eduardo
- Anselm, Irina
- Briere, Lauren C.
- High, Frances A.
- Sweetser, David A.
- Allard, Patrick
- Ashley, Euan A.
- Bacino, Carlos A.
- Baker, Eva
- Barseghyan, Hayk
- Batzli, Gabriel F.
- Behnam, Babak
- Bellen, Hugo J.
- Bernstein, Jonathan A.
- Bican, Anna
- Bostwick, Bret L.
- Brush, Matthew
- Burke, Elizabeth A.
- Burrage, Lindsay C.
- Butte, Manish J.
- Clark, Gary D.
- Colley, Heather A.
- Cooper, Cynthia M.
- Davids, Mariska
- Dell’Angelica, Esteban C.
- Dorrani, Naghmeh
- Douine, Emilie D.
- Emrick, Lisa T.
- Fairbrother, Laura
- Fernandez, Liliana
- Ferreira, Carlos
- Fieg, Elizabeth L.
- Fisher, Paul G.
- Friedman, Noah D.
- Gahl, William A.
- Gourdine, Jean‐Philippe F.
- Groden, Catherine A.
- Gropman, Andrea L.
- Haendel, Melissa
- Hom, Jason
- Howerton, Ellen M.
- Jamal, Fariha
- Jiang, Yong‐hui
- Johnston, Jean M.
- Jones, Angela L.
- Karaviti, Lefkothea
- Koeller, David M.
- Kohane, Isaac S.
- Koziura, Mary
- Lalani, Seema R.
- Lazar, Jozef
- Levy, Shawn E.
- Lincoln, Sharyn A.
- Maas, Richard L.
- Macnamara, Ellen F.
- MacRae, Calum A.
- Maduro, Valerie V.
- Majcherska, Marta M.
- Malicdan, May Christine V.
- Mamounas, Laura A.
- Manolio, Teri A.
- Markello, Thomas C.
- Marom, Ronit
- Martínez‐Agosto, Julian A.
- May, Thomas
- Morimoto, Marie
- Mulvihill, John J.
- Murphy, Jennifer L.
- Nelson, Stan F.
- Newman, John H.
- Novacic, Donna
- Orange, Jordan S.
- Potocki, Lorraine
- Reuter, Chloe M.
- Rives, Lynette
- Robertson, Amy K.
- Rodan, Lance H.
- Sampson, Jacinda B.
- Samson, Susan L.
- Schoch, Kelly
- Silverman, Edwin K.
- Sinsheimer, Janet S.
- Smith, Kevin S.
- Spillmann, Rebecca C.
- Stong, Nicholas
- Sullivan, Jennifer A.
- Waggott, Daryl M.
- Walsh, Chris A.
- Wangler, Michael F.
- Ward, Patricia A.
- Waters, Katrina M.
- Westerfield, Monte
- Wheeler, Matthew T.
- Wise, Anastasia L.
- Worthey, Elizabeth A.
- Yoon, Amanda J.
- Zastrow, Diane B.
2019
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Orphanet journal of rare diseases, 2021-05, Vol.16 (1), p.206-206, Article 206
2021
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Orphanet journal of rare diseases, 2017-04, Vol.12 (1), p.71-71, Article 71
2017
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Human molecular genetics, 2022-08, Vol.31 (17), p.2934-2950
- Barish, Scott
- Senturk, Mumine
- Schoch, Kelly
- Minogue, Amanda L
- Lopergolo, Diego
- Fallerini, Chiara
- Harland, Jake
- Seemann, Jacob H
- Stong, Nicholas
- Kranz, Peter G
- Kansagra, Sujay
- Mikati, Mohamad A
- Jasien, Joan
- El-Dairi, Mays
- Galluzzi, Paolo
- Ariani, Francesca
- Renieri, Alessandra
- Mari, Francesca
- Wangler, Michael F
- Arur, Swathi
- Jiang, Yong-Hui
- Yamamoto, Shinya
- Shashi, Vandana
- Bellen, Hugo J
2022
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Orphanet journal of rare diseases, 2023-01, Vol.18 (1), p.6-6, Article 6
2023
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BMC health services research, 2018-08, Vol.18 (1), p.652-652, Article 652
2018
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BMC bioinformatics, 2019-10, Vol.20 (1), p.496-496, Article 496
2019
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PLoS genetics, 2011-10, Vol.7 (10), p.e1002325-e1002325
- Pierson, Tyler Mark
- Adams, David
- Bonn, Florian
- Martinelli, Paola
- Cherukuri, Praveen F
- Teer, Jamie K
- Hansen, Nancy F
- Cruz, Pedro
- Mullikin For The Nisc Comparative Sequencing Program, James C
- Blakesley, Robert W
- Golas, Gretchen
- Kwan, Justin
- Sandler, Anthony
- Fuentes Fajardo, Karin
- Markello, Thomas
- Tifft, Cynthia
- Blackstone, Craig
- Rugarli, Elena I
- Langer, Thomas
- Gahl, William A
- Toro, Camilo
- Cox, Gregory A.
2011
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PLoS genetics, 2018-12, Vol.14 (12), p.e1007752-e1007752
- Cline, Melissa S
- Liao, Rachel G
- Parsons, Michael T
- Paten, Benedict
- Alquaddoomi, Faisal
- Antoniou, Antonis
- Baxter, Samantha
- Brody, Larry
- Cook-Deegan, Robert
- Coffin, Amy
- Couch, Fergus J
- Craft, Brian
- Currie, Robert
- Dlott, Chloe C
- Dolman, Lena
- den Dunnen, Johan T
- Dyke, Stephanie O M
- Domchek, Susan M
- Easton, Douglas
- Fischmann, Zachary
- Foulkes, William D
- Garber, Judy
- Goldgar, David
- Goldman, Mary J
- Goodhand, Peter
- Harrison, Steven
- Haussler, David
- Kato, Kazuto
- Knoppers, Bartha
- Markello, Charles
- Nussbaum, Robert
- Offit, Kenneth
- Plon, Sharon E
- Rashbass, Jem
- Rehm, Heidi L
- Robson, Mark
- Rubinstein, Wendy S
- Stoppa-Lyonnet, Dominique
- Tavtigian, Sean
- Thorogood, Adrian
- Zhang, Can
- Zimmermann, Marc
- Burn, John
- Chanock, Stephen
- Rätsch, Gunnar
- Spurdle, Amanda B
- Eng, Charis
2018
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Neuromuscular disorders : NMD, 2013-06, Vol.23 (6), p.483-488
- Pierson, Tyler Mark
- Markello, Thomas
- Accardi, John
- Wolfe, Lynne
- Adams, David
- Sincan, Murat
- Tarazi, Noor M
- Fajardo, Karin Fuentes
- Cherukuri, Praveen F
- Bajraktari, Ilda
- Meilleur, Katy G
- Donkervoort, Sandra
- Jain, Mina
- Hu, Ying
- Lehky, Tanya J
- Cruz, Pedro
- Mullikin, James C
- Bonnemann, Carsten
- Gahl, William A
- Boerkoel, Cornelius F
- Tifft, Cynthia J
2013
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Neurology, 2012-07, Vol.79 (2), p.123
2012
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