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Author/Creator Kent, Lindsey

1. A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Issue 12 (16th April 2021)

Authors:
Martinelli, Angela; Rice, Mabel L; Talcott, Joel B; Diaz, Rebeca; Smith, Shelley; Raza, Muhammad Hashim; Snowling, Margaret J; Hulme, Charles; Stein, John; Hayiou-Thomas, Marianna E; Hawi, Ziarih; Kent, Lindsey; Pitt, Samantha J; Newbury, Dianne F; Paracchini, Silvia
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 12(2021)
Page Start:
1160
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder. (17th November 2015)

Authors:
Tong, Janette; McKinley, Leigh-Anne; Cummins, Tarrant D.R.; Johnson, Beth; Matthews, Natasha; Vance, Alasdair; Heussler, Helen; Gill, Michael; Kent, Lindsey; Bellgrove, Mark A.; Hawi, Ziarih
Journal:
World journal of biological psychiatry
Issue:
Volume 16:Number 8(2015)
Page Start:
610
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. On the role of NOS1 ex1f‐VNTR in ADHD—allelic, subgroup, and meta‐analysis. Issue 6 (18th June 2015)

Authors:
Weber, Heike; Kittel‐Schneider, Sarah; Heupel, Julia; Weißflog, Lena; Kent, Lindsey; Freudenberg, Florian; Alttoa, Aet; Post, Antonia; Herterich, Sabine; Haavik, Jan; Halmøy, Anne; Fasmer, Ole B.; Landaas, Elisabeth T.; Johansson, Stefan; Cormand, Bru; Ribasés, Marta; Sánchez‐Mora, Cristina; Ramo...
Other Names:
Franke Barbara guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 168:Issue 6(2015)
Page Start:
445
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗