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Author/Creator Naidich, Thomas P.

2. Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor. Issue 6 (15th April 2021)

Authors:
Webb, Bryn D.; Evans, Anthony; Naidich, Thomas P.; Bird, Lynne M.; Parikh, Sumit; Fernandez Garcia, Meilin; Henderson, Lindsay B.; Millan, Francisca; Si, Yue; Brennand, Kristen J.; Hung, Peter; Rucker, Janet C.; Wheeler, Patricia G.; Schadt, Eric E.
Journal:
Human mutation
Issue:
Volume 42:Issue 6(2021)
Page Start:
685
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Novel, Compound Heterozygous, Single‐Nucleotide Variants in MARS2 Associated with Developmental Delay, Poor Growth, and Sensorineural Hearing Loss. Issue 6 (8th April 2015)

Authors:
Webb, Bryn D.; Wheeler, Patricia G.; Hagen, Jacob J.; Cohen, Ninette; Linderman, Michael D.; Diaz, George A.; Naidich, Thomas P.; Rodenburg, Richard J.; Houten, Sander M.; Schadt, Eric E.
Journal:
Human mutation
Issue:
Volume 36:Issue 6(2015:Jun.)
Page Start:
587
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Reproducibility of myelin content‐based human habenula segmentation at 3 Tesla. Issue 7 (26th March 2018)

Authors:
Kim, Joo‐Won; Naidich, Thomas P.; Joseph, Joshmi; Nair, Divya; Glasser, Matthew F.; O'halloran, Rafael; Doucet, Gaelle E.; Lee, Won Hee; Krinsky, Hannah; Paulino, Alejandro; Glahn, David C.; Anticevic, Alan; Frangou, Sophia; Xu, Junqian
Journal:
Human brain mapping
Issue:
Volume 39:Issue 7(2018)
Page Start:
3058
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗