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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 3
1966 1
1968 1
1969 2
1970 1
1971 1
1972 2
1979 1
1980 1
1981 2
1983 1
1985 4
1986 3
1987 7
1988 3
1989 5
1990 8
1991 7
1992 8
1993 3
1994 10
1995 2
1996 2
1997 1
1998 5
1999 5
2000 2
2001 10
2002 7
2003 4
2004 15
2005 15
2006 26
2007 18
2008 22
2009 27
2010 36
2011 41
2012 39
2013 36
2014 41
2015 33
2016 31
2017 40
2018 51
2019 62
2020 52
2021 64
2022 56
2023 43
2024 22

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Article attribute

Article type

Publication date

Search Results

776 results

Results by year

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Page 1
Investigation and management of Wilson's disease: a practical guide from the British Association for the Study of the Liver.
Shribman S, Marjot T, Sharif A, Vimalesvaran S, Ala A, Alexander G, Dhawan A, Dooley J, Gillett GT, Kelly D, McNeill A, Warner TT, Wheater V, Griffiths W, Bandmann O; British Association for the Study of the Liver Rare Diseases Special Interest Group. Shribman S, et al. Among authors: mcneill a. Lancet Gastroenterol Hepatol. 2022 Jun;7(6):560-575. doi: 10.1016/S2468-1253(22)00004-8. Epub 2022 Apr 13. Lancet Gastroenterol Hepatol. 2022. PMID: 35429442 Review.
Genes=disease (?).
McNeill A. McNeill A. Eur J Hum Genet. 2023 Mar;31(3):255-256. doi: 10.1038/s41431-023-01314-y. Eur J Hum Genet. 2023. PMID: 36890260 Free PMC article. No abstract available.
Clinical genetics-it's polygenic.
McNeill A. McNeill A. Eur J Hum Genet. 2021 Jul;29(7):1037. doi: 10.1038/s41431-021-00931-9. Eur J Hum Genet. 2021. PMID: 34267340 Free PMC article. No abstract available.
A Double-Blind, Randomized, Placebo-Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease.
Payne T, Appleby M, Buckley E, van Gelder LMA, Mullish BH, Sassani M, Dunning MJ, Hernandez D, Scholz SW, McNeill A, Libri V, Moll S, Marchesi JR, Taylor R, Su L, Mazzà C, Jenkins TM, Foltynie T, Bandmann O. Payne T, et al. Among authors: mcneill a. Mov Disord. 2023 Aug;38(8):1493-1502. doi: 10.1002/mds.29450. Epub 2023 May 29. Mov Disord. 2023. PMID: 37246815 Free article. Clinical Trial.
Using exomes better.
McNeill A. McNeill A. Eur J Hum Genet. 2024 Feb;32(2):138. doi: 10.1038/s41431-024-01539-5. Eur J Hum Genet. 2024. PMID: 38332348 No abstract available.
Clinical genomics-but faster.
McNeill A. McNeill A. Eur J Hum Genet. 2021 Jun;29(6):889-890. doi: 10.1038/s41431-021-00906-w. Eur J Hum Genet. 2021. PMID: 34006928 Free PMC article. No abstract available.
A new system for variant classification?
McNeill A. McNeill A. Eur J Hum Genet. 2022 Feb;30(2):137-138. doi: 10.1038/s41431-021-01032-3. Eur J Hum Genet. 2022. PMID: 35132196 Free PMC article. No abstract available.
Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders.
Levy MA, Relator R, McConkey H, Pranckeviciene E, Kerkhof J, Barat-Houari M, Bargiacchi S, Biamino E, Palomares Bralo M, Cappuccio G, Ciolfi A, Clarke A, DuPont BR, Elting MW, Faivre L, Fee T, Ferilli M, Fletcher RS, Cherick F, Foroutan A, Friez MJ, Gervasini C, Haghshenas S, Hilton BA, Jenkins Z, Kaur S, Lewis S, Louie RJ, Maitz S, Milani D, Morgan AT, Oegema R, Østergaard E, Pallares NR, Piccione M, Plomp AS, Poulton C, Reilly J, Rius R, Robertson S, Rooney K, Rousseau J, Santen GWE, Santos-Simarro F, Schijns J, Squeo GM, John MS, Thauvin-Robinet C, Traficante G, van der Sluijs PJ, Vergano SA, Vos N, Walden KK, Azmanov D, Balci TB, Banka S, Gecz J, Henneman P, Lee JA, Mannens MMAM, Roscioli T, Siu V, Amor DJ, Baynam G, Bend EG, Boycott K, Brunetti-Pierri N, Campeau PM, Campion D, Christodoulou J, Dyment D, Esber N, Fahrner JA, Fleming MD, Genevieve D, Heron D, Husson T, Kernohan KD, McNeill A, Menke LA, Merla G, Prontera P, Rockman-Greenberg C, Schwartz C, Skinner SA, Stevenson RE, Vincent M, Vitobello A, Tartaglia M, Alders M, Tedder ML, Sadikovic B. Levy MA, et al. Among authors: mcneill a. Hum Mutat. 2022 Nov;43(11):1609-1628. doi: 10.1002/humu.24446. Epub 2022 Aug 21. Hum Mutat. 2022. PMID: 35904121
776 results