David Curtis

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 33

Top Venues

Annals of human genetics

The British journal of psychiatry : the journal of mental science

PLoS genetics

Journal of human genetics

Queen Mary University of London

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Queen Mary University of London Jan 01 2016

United Kingdom

Honorary Professor :: Centre for Psychiatry

University College London Dec 01 2011

United Kingdom

Honorary Professor :: UCL Genetics Institute

Publications

David Curtis
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia risk. Journal of human genetics 69 (6) (2024)
David Curtis
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia risk. Journal of human genetics 69 (6) (2024)
David Curtis
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia risk. Journal of human genetics 69 (6) (2024)
David Curtis
Assessment of ability of AlphaMissense to identify variants affecting susceptibility to common disease. European journal of human genetics : EJHG (2024)
David Curtis
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia risk. Journal of human genetics (2024)
David Curtis
Opinion: Increased calorie gain from lactose digestion could contribute to selection for lactase persistence. PLoS genetics 19 (2) (2023)
David Curtis
Social scientists would do well to steer clear of polygenic scores. The Behavioral and brain sciences 46 (2023)
David Curtis
Opinion: Increased calorie gain from lactose digestion could contribute to selection for lactase persistence. PLoS genetics 19 (2) (2023)
David Curtis, William Amos
The human genome harbours widespread exclusive yin yang haplotypes. European journal of human genetics : EJHG (2023)
David Curtis
Opinion: Increased calorie gain from lactose digestion could contribute to selection for lactase persistence. PLoS genetics 19 (2) (2023)
David Curtis
Opinion: Increased calorie gain from lactose digestion could contribute to selection for lactase persistence. PLoS genetics 19 (2) (2023)
David Curtis
Opinion: Increased calorie gain from lactose digestion could contribute to selection for lactase persistence. PLoS genetics 19 (2) (2023)
David Curtis
Weighted burden analysis in 200,000 exome-sequenced subjects characterises rare variant effects on BMI. International journal of obesity (2005) 46 (4) (2022)
David Curtis
RE: Extending the vulnerability-stress model of mental disorders: three-dimensional NPSR1 × environment × coping interaction study in anxiety. The British journal of psychiatry : the journal of mental science 222 (1) (2022)
David Curtis
Identification of specific genes involved in schizophrenia aetiology - what difference does it make? The British journal of psychiatry : the journal of mental science 221 (2) (2022)
Duncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, Rolf Adolfsson, Nick Bass, Douglas H R Blackwood, Marco P M Boks, Chia-Yen Chen, Claire Churchhouse, Aiden P Corvin, Nicholas Craddock, David Curtis, Arianna Di Florio, Faith Dickerson, Nelson A Freimer, Fernando S Goes, Xiaoming Jia, Ian R Jones, Lisa A Jones, Lina Jonsson, Rene S Kahn, Mikaél Landén, Adam E Locke, Andrew M McIntosh, Andrew McQuillin, Derek W Morris, Michael C O'Donovan, Roel A Ophoff, Michael J Owen, Nancy L Pedersen, Danielle Posthuma, Andreas Reif, Neil Risch, Catherine Schaefer, Laura J Scott, Tarjinder Singh, Jordan W Smoller, Matthew Solomonson, David St Clair, Eli A Stahl, Annabel Vreeker, James T R Walters, Weiqing Wang, Nicholas A Watts, Robert Yolken, Peter P Zandi, Benjamin M Neale
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. Nature genetics 54 (5) (2022)
David Curtis
RE: Extending the vulnerability-stress model of mental disorders: three-dimensional NPSR1 × environment × coping interaction study in anxiety. The British journal of psychiatry : the journal of mental science 222 (1) (2022)
David Curtis, null null
Analysis of whole genome sequenced cases and controls shows that the association of variants in TOMM40, BCAM, NECTIN2 and APOC1 with late onset Alzheimer's disease is driven by linkage disequilibrium with APOE ε2/ε3/ε4 alleles. Journal of neurogenetics 35 (2) (2021)
David Curtis
Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes. Diabetes/metabolism research and reviews (2021)
Emma N Hilton, Pam Thompson, Colin Wright, David Curtis
The reality of sex. Irish journal of medical science 190 (4) (2021)
David Curtis
Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia. Journal of medical genetics (2021)
David Curtis, Kaushiki Bakaya, Leona Sharma, Sreejan Bandyopadhyay
Weighted burden analysis of exome-sequenced late-onset Alzheimer's cases and controls provides further evidence for a role for PSEN1 and suggests involvement of the PI3K/Akt/GSK-3β and WNT signalling pathways. Annals of human genetics 84 (3) (2020)
Eszter Balogh, Jennifer C Chandler, Máté Varga, Mona Tahoun, Dóra K Menyhárd, Gusztáv Schay, Tomas Goncalves, Renáta Hamar, Regina Légrádi, Ákos Szekeres, Olivier Gribouval, Robert Kleta, Horia Stanescu, Detlef Bockenhauer, Andrea Kerti, Hywel Williams, Veronica Kinsler, Wei-Li Di, David Curtis, Maria Kolatsi-Joannou, Hafsa Hammid, Anna Szőcs, Kristóf Perczel, Erika Maka, Gergely Toldi, Florentina Sava, Christelle Arrondel, Magdolna Kardos, Attila Fintha, Ahmed Hossain, Felice D'Arco, Marios Kaliakatsos, Jutta Koeglmeier, William Mifsud, Mariya Moosajee, Ana Faro, Eszter Jávorszky, Gábor Rudas, Marwa H Saied, Salah Marzouk, Kata Kelen, Judit Götze, George S Reusz, Tivadar Tulassay, François Dragon, Geraldine Mollet, Susanne Motameny, Holger Thiele, Guillaume Dorval, Peter Nürnberg, András Perczel, Attila J Szabo, David A Long, Kazunori Tomita, Corinne Antignac, Aoife M Waters, Kálmán Tory
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. Proceedings of the National Academy of Sciences of the United States of America 117 (26) (2020)
David Curtis
A possible role for sarcosine in the management of schizophrenia. The British journal of psychiatry : the journal of mental science 215 (6) (2020)
Mason Alexander, David Curtis
LD scores are associated with differences in allele frequencies between populations but LD score regression can still distinguish confounding from polygenicity. Annals of human genetics 84 (5) (2020)
David Curtis
Clinical relevance of genome-wide polygenic score may be less than claimed. Annals of human genetics 83 (4) (2019)
David Curtis, Katherine Adlington, Kamaldeep S Bhui
Pursuing parity: genetic tests for psychiatric conditions in the UK National Health Service. The British journal of psychiatry : the journal of mental science 214 (5) (2019)
Ney Alliey-Rodriguez, Tamar A Grey, Rebecca Shafee, Huma Asif, Olivia Lutz, Nicolas R Bolo, Jaya Padmanabhan, Neeraj Tandon, Madeline Klinger, Katherine Reis, Jonathan Spring, Lucas Coppes, Victor Zeng, Rachal R Hegde, Dung T Hoang, Deepthi Bannai, Uzma Nawaz, Philip Henson, Siyuan Liu, Diane Gage, Steven McCarroll, Jeffrey R Bishop, Scot Hill, James L Reilly, Rebekka Lencer, Brett A Clementz, Peter Buckley, David C Glahn, Shashwath A Meda, Balaji Narayanan, Godfrey Pearlson, Matcheri S Keshavan, Elena I Ivleva, Carol Tamminga, John A Sweeney, David Curtis, Judith A Badner, Sarah Keedy, Judith Rapoport, Yanling Liu, Elliot S Gershon
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Translational psychiatry 9 (1) (2019)
Jonathan L Hess, Daniel S Tylee, Manuel Mattheisen, null null, null null, Anders Dupont Børglum, Thomas Damm Als, Jakob Grove, Thomas Werge, Preben Bo Mortensen, Ole Mors, Merete Nordentoft, David Michael Hougaard, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Tiffany A Greenwood, Ming T Tsuang, David Curtis, Stacy Steinberg, Engilbert Sigurdsson, Hreinn Stefánsson, Kári Stefánsson, Howard J Edenberg, Peter Holmans, Stephen V Faraone, Stephen J Glatt
A polygenic resilience score moderates the genetic risk for schizophrenia. Molecular psychiatry 26 (3) (2019)
Leda Coelewij, David Curtis
Mini-review: Update on the genetics of schizophrenia. Annals of human genetics 82 (5) (2018)
David Curtis, Leda Coelewij, Shou-Hwa Liu, Jack Humphrey, Richard Mott
Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology. Behavior genetics 48 (3) (2018)
David Curtis
Construction of an Exome-Wide Risk Score for Schizophrenia Based on a Weighted Burden Test. Annals of human genetics 82 (1) (2017)
Mariam M Al Eissa, Alessia Fiorentino, Sally I Sharp, Niamh L O'Brien, Kate Wolfe, Giovanni Giaroli, David Curtis, Nicholas J Bass, Andrew McQuillin
Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. Annals of human genetics 82 (2) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

David Curtis