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Author/Creator Scott, Hamish S.

1. A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability. (3rd June 2020)

Authors:
Fox, Lucy C.; Tan, Michelle; Brown, Anna L.; Arts, Peer; Thompson, Ella; Ryland, Georgina L.; Lickiss, Jennifer; Scott, Hamish S.; Poplawski, Nicola K.; Phillips, Kerry; Came, Neil A.; James, Paul; Ting, Stephen B.; Ritchie, David S.; Szer, Jeff; Hahn, Christopher N.; Schwarer, Anthony; Blombery,...
Journal:
British journal of haematology
Issue:
Volume 190:Number 5(2020)
Page Start:
e297
Record Type:
Journal Article
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3. Apparent 'JAK2‐negative' polycythaemia vera due to compound mutations in exon 14. (2nd May 2016)

Authors:
Tiong, Ing Soo; Casolari, Debora A.; Moore, Sarah; Nguyen, Tran; Van Velzen, Merel J. M.; Zantomio, Daniela; Scott, Hamish S.; D'Andrea, Richard J.; Hahn, Christopher N.; Ross, David M.
Journal:
British journal of haematology
Issue:
Volume 178:Number 2(2017)
Page Start:
333
Record Type:
Journal Article
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4. Autoimmune hepatitis in a murine autoimmune polyendocrine syndrome type 1 model is directed against multiple autoantigens. Issue 4 (24th February 2015)

Authors:
Hardtke‐Wolenski, Matthias; Taubert, Richard; Noyan, Fatih; Sievers, Maren; Dywicki, Janine; Schlue, Jerome; Falk, Christine S.; Ardesjö Lundgren, Brita; Scott, Hamish S.; Pich, Andreas; Anderson, Mark S.; Manns, Michael P.; Jaeckel, Elmar
Journal:
Hepatology
Issue:
Volume 61:Issue 4(2015:Apr.)
Page Start:
1295
Record Type:
Journal Article
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6. Brief Report: Identification of a Pathogenic Variant in TREX1 in Early‐Onset Cerebral Systemic Lupus Erythematosus by Whole‐Exome Sequencing. Issue 12 (December 2014)

Authors:
Ellyard, Julia I.; Jerjen, Rebekka; Martin, Jaime L.; Lee, Adrian Y. S.; Field, Matthew A.; Jiang, Simon H.; Cappello, Jean; Naumann, Svenja K.; Andrews, T. Daniel; Scott, Hamish S.; Casarotto, Marco G.; Goodnow, Christopher C.; Chaitow, Jeffrey; Pascual, Virginia; Hertzog, Paul; Alexander, Steph...
Journal:
Arthritis & rheumatology
Issue:
Volume 66:Issue 12(2014)
Page Start:
3382
Record Type:
Journal Article
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8. Cover Image, Volume 37, Issue 9. Issue 9 (September 2016)

Authors:
Barnett, Christopher P.; Nataren, Nathalie J.; Klingler‐Hoffmann, Manuela; Schwarz, Quenten; Chong, Chan‐Eng; Lee, Young K.; Bruno, Damien L.; Lipsett, Jill; McPhee, Andrew J.; Schreiber, Andreas W.; Feng, Jinghua; Hahn, Christopher N.; Scott, Hamish S.
Journal:
Human mutation
Issue:
Volume 37:Issue 9(2016)
Page Start:
i
Record Type:
Journal Article
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10. Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing. Issue 9 (11th July 2016)

Authors:
Barnett, Christopher P.; Nataren, Nathalie J.; Klingler‐Hoffmann, Manuela; Schwarz, Quenten; Chong, Chan‐Eng; Lee, Young K.; Bruno, Damien L.; Lipsett, Jill; McPhee, Andrew J.; Schreiber, Andreas W.; Feng, Jinghua; Hahn, Christopher N.; Scott, Hamish S.
Journal:
Human mutation
Issue:
Volume 37:Issue 9(2016)
Page Start:
955
Record Type:
Journal Article
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