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Author/Creator Taylor, Martin S.

1. A CGG‐Repeat Expansion Mutation in ZNF713 Causes FRA7A: Association with Autistic Spectrum Disorder in Two Families. Issue 11 (November 2014)

Authors:
Metsu, Sofie; Rainger, Jacqueline K.; Debacker, Kim; Bernhard, Birgitta; Rooms, Liesbeth; Grafodatskaya, Daria; Weksberg, Rosanna; Fombonne, Eric; Taylor, Martin S.; Scherer, Stephen W.; Kooy, R. Frank; FitzPatrick, David R.
Journal:
Human mutation
Issue:
Volume 35:Issue 11(2014:Nov.)
Page Start:
1295
Record Type:
Journal Article
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2. Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model. Issue 22 (2nd November 2017)

Authors:
Moss, Chloe F.; Dalla Rosa, Ilaria; Hunt, Lilian E.; Yasukawa, Takehiro; Young, Robert; Jones, Aleck W. E.; Reddy, Kaalak; Desai, Radha; Virtue, Sam; Elgar, Greg; Voshol, Peter; Taylor, Martin S.; Holt, Ian J.; Reijns, Martin A. M.; Spinazzola, Antonella
Journal:
Nucleic acids research
Issue:
Volume 45:Issue 22(2017)
Page Start:
12808
Record Type:
Journal Article
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4. Exome Sequencing to Detect Rare Variants Associated With General Cognitive Ability: A Pilot Study. (6th March 2015)

Authors:
Luciano, Michelle; Svinti, Victoria; Campbell, Archie; Marioni, Riccardo E.; Hayward, Caroline; Wright, Alan F.; Taylor, Martin S.; Porteous, David J.; Thomson, Pippa; Prendergast, James G.D.; Hastie, Nicholas D.; Farrington, Susan M.; Scotland, Generation; Dunlop, Malcolm G.; Deary, Ian J.
Journal:
Twin research and human genetics
Issue:
Volume 18:Number 2(2015)
Page Start:
117
Record Type:
Journal Article
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5. High Prevalence and Disease Correlation of Autoantibodies Against p40 Encoded by Long Interspersed Nuclear Elements in Systemic Lupus Erythematosus. Issue 1 (27th December 2019)

Authors:
Carter, Victoria; LaCava, John; Taylor, Martin S.; Liang, Shu Ying; Mustelin, Cecilia; Ukadike, Kennedy C.; Bengtsson, Anders; Lood, Christian; Mustelin, Tomas
Journal:
Arthritis & rheumatology
Issue:
Volume 72:Issue 1(2020)
Page Start:
89
Record Type:
Journal Article
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6. Immune‐Related Adverse Events in the Setting of PD‐1/L1 Inhibitor Combination Therapy. (21st November 2019)

Authors:
Zubiri, Leyre; Allen, Ian M.; Taylor, Martin S.; Guidon, Amanda C.; Chen, Steven T.; Schoenfeld, Sara R.; Neilan, Tomas G.; Sise, Meghan E.; Mooradian, Meghan J.; Rubin, Krista M.; Leaf, Rebecca Karp; Parikh, Aparna R.; Faje, Alexander; Gainor, Justin F.; Cohen, Justine V.; Fintelmann, Florian J....
Journal:
Oncologist
Issue:
Volume 25:Number 3(2020)
Page Start:
e398
Record Type:
Journal Article
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8. LGR5 in Barrett's Esophagus and its Utility in Predicting Patients at Increased Risk of Advanced Neoplasia. Issue 1 (22nd January 2021)

Authors:
Neyaz, Azfar; Odze, Robert D.; Rickelt, Steffen; Nieman, Linda T.; Bledsoe, Jacob R.; Mahadevan, Krishnan K.; Arora, Kshitij; Jeck, William R.; Taylor, Martin S.; Gala, Manish; Patil, Deepa T.; Yilmaz, Omer H.; Rivera, Miguel N.; Ting, David T.; Deshpande, Vikram
Journal:
Clinical and translational gastroenterology
Issue:
Volume 12:Issue 1(2021)
Page Start:
e00272
Record Type:
Journal Article
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9. Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. Issue 4 (11th March 2014)

Authors:
Handley, Mark T.; Mégarbané, André; Meynert, Alison M.; Brown, Stephen; Freyer, Elisabeth; Taylor, Martin S.; Jackson, Ian J.; Aligianis, Irene A.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 2:Issue 4(2014:Jul.)
Page Start:
319
Record Type:
Journal Article
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