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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 57
2023 7
Text availability
Article attribute
Article type
Publication date

Search Results

723 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.
Vaping in Pregnancy: A Systematic Review.
Calder R, Gant E, Bauld L, McNeill A, Robson D, Brose LS. Calder R, et al. Among authors: mcneill a. Nicotine Tob Res. 2021 Aug 18;23(9):1451-1458. doi: 10.1093/ntr/ntab017. Nicotine Tob Res. 2021. PMID: 33538828 Free PMC article.
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.
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders.
Levy MA, McConkey H, Kerkhof J, Barat-Houari M, Bargiacchi S, Biamino E, Bralo MP, Cappuccio G, Ciolfi A, Clarke A, DuPont BR, Elting MW, Faivre L, Fee T, Fletcher RS, Cherik 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, Pizzi S, Plomp AS, Poulton C, Reilly J, Relator R, Rius R, Robertson S, Rooney K, Rousseau J, Santen GWE, Santos-Simarro F, Schijns J, Squeo GM, St John M, Thauvin-Robinet C, Traficante G, van der Sluijs PJ, Vergano SA, Vos N, Walden KK, Azmanov D, Balci T, 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, Christodoulou J, Dyment D, Esber N, Fahrner JA, Fleming MD, Genevieve D, Kerrnohan KD, McNeill A, Menke LA, Merla G, Prontera P, Rockman-Greenberg C, Schwartz C, Skinner SA, Stevenson RE, Vitobello A, Tartaglia M, Alders M, Tedder ML, Sadikovic B. Levy MA, et al. Among authors: mcneill a. HGG Adv. 2021 Dec 3;3(1):100075. doi: 10.1016/j.xhgg.2021.100075. eCollection 2022 Jan 13. HGG Adv. 2021. PMID: 35047860 Free PMC article.
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.
New year, new issue.
McNeill A. McNeill A. Eur J Hum Genet. 2022 Jan;30(1):1-2. doi: 10.1038/s41431-021-01014-5. Eur J Hum Genet. 2022. PMID: 34848845 Free PMC article. No abstract available.
Out now in May's EJHG.
McNeill A. McNeill A. Eur J Hum Genet. 2021 May;29(5):721. doi: 10.1038/s41431-021-00896-9. Eur J Hum Genet. 2021. PMID: 33972741 Free PMC article. No abstract available.
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile.
Al-Jawahiri R, Foroutan A, Kerkhof J, McConkey H, Levy M, Haghshenas S, Rooney K, Turner J, Shears D, Holder M, Lefroy H, Castle B, Reis LM, Semina EV; University of Washington Centre for Mendelian Genomics (UW-CMG); Lachlan K, Chandler K, Wright T, Clayton-Smith J, Hug FP, Pitteloud N, Bartoloni L, Hoffjan S, Park SM, Thankamony A, Lees M, Wakeling E, Naik S, Hanker B, Girisha KM, Agolini E, Giuseppe Z, Alban Z, Tessarech M, Keren B, Afenjar A, Zweier C, Reis A, Smol T, Tsurusaki Y, Nobuhiko O, Sekiguchi F, Tsuchida N, Matsumoto N, Kou I, Yonezawa Y, Ikegawa S, Callewaert B, Freeth M; Genomics England Research Consortium; Kleinendorst L, Donaldson A, Alders M, De Paepe A, Sadikovic B, McNeill A. Al-Jawahiri R, et al. Among authors: mcneill a. Genet Med. 2022 Jun;24(6):1261-1273. doi: 10.1016/j.gim.2022.02.013. Epub 2022 Mar 24. Genet Med. 2022. PMID: 35341651 Free PMC article.
723 results