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Andrew G. McKechanie

Observed names: A. G. McKechanie, A. McKechanie, Andrew G McKechanie, Andrew McKechanie, Andrew G. McKechanie, McKechanie, Andrew, McKechanie, Andrew G., McKechanie, Andrew Graeme, McKechanie, Andrew; id_orcid 0000-0003-4273-9906
Observed institutions: Northwestern University, NHS Lothian, Royal Edinburgh Hospital, Duchess Of Kent Hospital, Simons Initiative for the Developing Brain, University College London, Cardiff University, University of Edinburgh
ORCID: 0000-0003-4273-9906
Observed ORCID: 0000-0003-4273-9906
OpenAlex ID: A5037514607
The UK10K project identifies rare variants in health and disease
2015 · Writing group, Klaudia Walter, et al. · Nature · 1,053
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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
2015 · Jie Huang, Bryan Howie, et al. · Nature Communications · 348
Correction: Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
2016 · Miriam Schmidts, Yuqing Hou, et al. · Nature Communications · 267
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Synaptic scaffold evolution generated components of vertebrate cognitive complexity
2012 · Jess Nithianantharajah, Noboru H Komiyama, et al. · Nature Neuroscience · 265
Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS)
2015 · Ana Maria Fernandez-Pujals, Mark James Adams, et al. · PLoS ONE · 134
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Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene
2015 · J. Nithianantharajah, A. G. McKechanie, et al. · Scientific Reports · 122
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Whole-genome sequence-based analysis of thyroid function
2015 · Peter N. Taylor, Eleonora Porcu, et al. · Nature Communications · 107
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The perspectives of stakeholders of intellectual disability liaison nurses: a model of compassionate, person‐centred care
2016 · Michael Brown, Zoë Chouliara, et al. · Journal of Clinical Nursing · 106
Making reasonable and achievable adjustments: the contributions of learning disability liaison nurses in ‘Getting it right’ for people with learning disabilities receiving general hospitals care
2015 · Juliet MacArthur, Michael Brown, et al. · Journal of Advanced Nursing · 91
Learning Disability Liaison Nursing Services in south‐east Scotland: a mixed‐methods impact and outcome study
2011 · M. Brown, J. MacArthur, et al. · Journal of Intellectual Disability Research · 78
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
2017 · Audrey E. Hendricks, Elena G. Bochukova, et al. · Scientific Reports · 76
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TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
2015 · Miriam Schmidts, Yuqing Hou, et al. · Nature Communications · 73
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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
2014 · Nicholas J. Timpson, Klaudia Walter, et al. · Nature Communications · 71
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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
2019 · Kathleen M. Gorman, Esther Meyer, et al. · The American Journal of Human Genetics · 67
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Acute military psychiatric casualties from the war in Iraq
2005 · Mark A. Turner, Mathew D. Kiernan, et al. · The British Journal of Psychiatry · 58
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Facial emotion recognition in Scottish prisoners
2011 · Louise Robinson, Michael D. Spencer, et al. · International Journal of Law and Psychiatry · 37
Clinical and behavioural features of SYNGAP1-related intellectual disability: a parent and caregiver description
2022 · Damien Wright, Aisling Kenny, et al. · Journal of Neurodevelopmental Disorders · 35
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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
2019 · Simon Haworth, Chin Yang Shapland, et al. · Nature Communications · 35
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Equality and access to general health care for people with learning disabilities: reality or rhetoric?
2010 · Michael Brown, Juliet MacArthur, et al. · Journal of research in nursing · 29
Negative symptoms and longitudinal grey matter tissue loss in adolescents at risk of psychosis: Preliminary findings from a 6-year follow-up study
2015 · Andrew G. McKechanie, Thomas W. J. Moorhead, et al. · The British Journal of Psychiatry · 27
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Links between Autism Spectrum Disorder Diagnostic Status and Family Quality of Life
2017 · Andrew McKechanie, Vivien Moffat, et al. · Children · 25
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A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability
2013 · Eske M. Derks, Muhammad Ayub, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 24
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Sexual health services and support: The views of younger adults with intellectual disability
2014 · Fionnuala Williams, Gordon Scott, et al. · Journal of Intellectual & Developmental Disability · 23
Lived experiences of depression in autistic children and adolescents: A qualitative study on child and parent perspectives
2023 · Sinead M. Rhodes, Christopher B. Eaton, et al. · Research in Developmental Disabilities · 20
A holistic approach to fragile X syndrome integrated guidance for person‐centred care
2024 · Kirsten Johnson, Andrew C. Stanfield, et al. · Journal of Applied Research in Intellectual Disabilities · 12
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Works count: 66
Citation count: 3,308
H-index: 23
I10-index: 30
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