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Author/Creator Standridge, Shannon

1. Analysis of X‐inactivation status in a Rett syndrome natural history study cohort. Issue 5 (23rd March 2022)

Authors:
Fang, Xiaolan; Butler, Kameryn M.; Abidi, Fatima; Gass, Jennifer; Beisang, Arthur; Feyma, Timothy; Ryther, Robin C.; Standridge, Shannon; Heydemann, Peter; Jones, Mary; Haas, Richard; Lieberman, David N; Marsh, Eric D.; Benke, Tim A.; Skinner, Steve; Neul, Jeffrey L.; Percy, Alan K.; Friez, ...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 10:Issue 5(2022)
Page Start:
n/a
Record Type:
Journal Article
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2. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Issue 5 (15th March 2019)

Authors:
Peters, Sarika U.; Fu, Cary; Suter, Bernhard; Marsh, Eric; Benke, Timothy A.; Skinner, Steve A.; Lieberman, David N.; Standridge, Shannon; Jones, Mary; Beisang, Arthur; Feyma, Timothy; Heydeman, Peter; Ryther, Robin; Kaufmann, Walter E.; Glaze, Daniel G.; Neul, Jeffrey L.; Percy, Alan K.
Journal:
Clinical genetics
Issue:
Volume 95:Issue 5(2019)
Page Start:
575
Record Type:
Journal Article
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3. Consensus guidelines on managing Rett syndrome across the lifespan. Issue 1 (13th September 2020)

Authors:
Fu, Cary; Armstrong, Dallas; Marsh, Eric; Lieberman, David; Motil, Kathleen; Witt, Rochelle; Standridge, Shannon; Nues, Paige; Lane, Jane; Dinkel, Tristen; Coenraads, Monica; von Hehn, Jana; Jones, Mary; Hale, Katie; Suter, Bernhard; Glaze, Daniel; Neul, Jeffrey; Percy, Alan; Benke, Timothy
Journal:
BMJ paediatrics open
Issue:
Volume 4:Issue 1(2020)
Page Start:
Record Type:
Journal Article
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4. Multisystem comorbidities in classic Rett syndrome: a scoping review. Issue 1 (22nd September 2020)

Authors:
Fu, Cary; Armstrong, Dallas; Marsh, Eric; Lieberman, David; Motil, Kathleen; Witt, Rochelle; Standridge, Shannon; Lane, Jane; Dinkel, Tristen; Jones, Mary; Hale, Katie; Suter, Bernhard; Glaze, Daniel; Neul, Jeffrey; Percy, Alan; Benke, Timothy
Journal:
BMJ paediatrics open
Issue:
Volume 4:Issue 1(2020)
Page Start:
Record Type:
Journal Article
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5. Phenotypic features in MECP2 duplication syndrome: Effects of age. Issue 2 (10th November 2020)

Authors:
Peters, Sarika U.; Fu, Cary; Marsh, Eric D.; Benke, Tim A.; Suter, Bernard; Skinner, Steve A.; Lieberman, David N.; Standridge, Shannon; Jones, Mary; Beisang, Arthur; Feyma, Timothy; Heydeman, Peter; Ryther, Robin; Glaze, Daniel G.; Percy, Alan K.; Neul, Jeffrey L.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 2(2021)
Page Start:
362
Record Type:
Journal Article
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6. The array of clinical phenotypes of males with mutations in Methyl‐CpG binding protein 2. Issue 1 (7th December 2018)

Authors:
Neul, Jeffrey L.; Benke, Timothy A.; Marsh, Eric D.; Skinner, Steven A.; Merritt, Jonathan; Lieberman, David N.; Standridge, Shannon; Feyma, Timothy; Heydemann, Peter; Peters, Sarika; Ryther, Robin; Jones, Mary; Suter, Bernhard; Kaufmann, Walter E.; Glaze, Daniel G.; Percy, Alan K.
Journal:
American journal of medical genetics
Issue:
Volume 180:Issue 1(2019)
Page Start:
55
Record Type:
Journal Article
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