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Author/Creator Craig, David W.

2. A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41‐q42 deletion phenotype. Issue 7 (16th July 2018)

Authors:
Balak, Chris; Belnap, Newell; Ramsey, Keri; Joss, Shelagh; Devriendt, Koen; Naymik, Marcus; Jepsen, Wayne; Siniard, Ashley L.; Szelinger, Szabolcs; Parker, Mary E.; Richholt, Ryan; Izatt, Tyler; LaFleur, Madison; Terraf, Panieh; Llaci, Lorida; De Both, Matt; Piras, Ignazio S.; Rangasamy, Sampathk...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 7(2018)
Page Start:
1549
Record Type:
Journal Article
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3. Characterisation of age and polarity at onset in bipolar disorder. (December 2021)

Authors:
Kalman, Janos L.; Olde Loohuis, Loes M.; Vreeker, Annabel; McQuillin, Andrew; Stahl, Eli A.; Ruderfer, Douglas; Grigoroiu-Serbanescu, Maria; Panagiotaropoulou, Georgia; Ripke, Stephan; Bigdeli, Tim B.; Stein, Frederike; Meller, Tina; Meinert, Susanne; Pelin, Helena; Streit, Fabian; Papiol, Sergi;...
Other Names:
collab.; collab.; collab.
Journal:
British journal of psychiatry
Issue:
Volume 219:Number 6(2021)
Page Start:
659
Record Type:
Journal Article
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4. Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1. (August 2020)

Authors:
Szelinger, Szabolcs; Krate, Jonida; Ramsey, Keri; Strom, Samuel P.; Shieh, Perry B.; Lee, Hane; Belnap, Newell; Balak, Chris; Siniard, Ashley L.; Russell, Megan; Richholt, Ryan; Both, Matt De; Claasen, Ana M.; Schrauwen, Isabelle; Nelson, Stanley F.; Huentelman, Matthew J.; Craig, David W.; Yang,...
Journal:
Neurology
Issue:
Volume 6:Number 4(2020)
Page Start:
Record Type:
Journal Article
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6. Extramedullary myeloma whole genome sequencing reveals novel mutations in Cereblon, proteasome subunit G2 and the glucocorticoid receptor in multi drug resistant disease. (11th March 2013)

Authors:
Egan, Jan B.; Kortuem, K. Martin; Kurdoglu, Ahmet; Izatt, Tyler; Aldrich, Jessica; Reiman, Rebecca; Phillips, Lori; Baker, Angela; Shi, Chang‐Xin; Schmidt, Jessica; Liang, Winnie S.; Craig, David W.; Carpten, John D.; Stewart, A. Keith
Journal:
British journal of haematology
Issue:
Volume 161:Number 5(2013:Jun.)
Page Start:
748
Record Type:
Journal Article
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8. Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. (2nd June 2011)

Authors:
Swaminathan, Shanker; Kim, Sungeun; Shen, Li; Risacher, Shannon L.; Foroud, Tatiana; Pankratz, Nathan; Potkin, Steven G.; Huentelman, Matthew J.; Craig, David W.; Weiner, Michael W.; Saykin, Andrew J.; (ADNI), The Alzheimer's Disease Neuroimaging Initiative
Other Names:
Nacmias Benedetta Academic Editor.
Journal:
International journal of alzheimer's disease
Issue:
Volume 2011(2011)
Page Start:
Record Type:
Journal Article
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9. LRP10 in α-synucleinopathies. Issue 12 (December 2018)

Authors:
Kia, Demis A; Sabir, Marya S; Ahmed, Sarah; Trinh, Joanne; Bandres-Ciga, Sara; Noyce, Alastair J; Kaiyrzhanov, Rauan; Middlehurst, Ben; Kia, Demis A; Tan, Manuela; Houlden, Henry; Morris, Huw R; Plun-Favreau, Helene; Holmans, Peter; Hardy, John; Trabzuni, Daniah; Bras, Jose; Quinn, John; Mok, Kin...
Journal:
Lancet neurology
Issue:
Volume 17:Issue 12(2018)
Page Start:
1032
Record Type:
Journal Article
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