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

Year Number of Results
1950 1
1961 1
1971 4
1972 2
1975 2
1976 2
1977 2
1979 2
1980 4
1981 3
1982 3
1983 3
1984 2
1985 2
1986 5
1987 3
1988 2
1989 1
1990 4
1991 6
1992 3
1993 7
1994 1
1995 4
1996 1
1997 1
1998 5
1999 3
2000 6
2001 2
2002 6
2003 2
2004 7
2005 6
2006 15
2007 8
2008 7
2009 7
2010 3
2011 9
2012 6
2013 5
2015 2
2016 1
2017 1
2018 5
2019 4
2020 2
2021 5
2022 2
2023 1
2024 2
2025 0

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189 results

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Page 1
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Among authors: maclennan ah. Nat Genet. 2020 Oct;52(10):1046-1056. doi: 10.1038/s41588-020-0695-1. Epub 2020 Sep 28. Nat Genet. 2020. PMID: 32989326 Free PMC article.
Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.
Wang Y, Xu Y, Zhou C, Cheng Y, Qiao N, Shang Q, Xia L, Song J, Gao C, Qiao Y, Zhang X, Li M, Ma C, Fan Y, Peng X, Wu S, Lv N, Li B, Sun Y, Zhang B, Li T, Li H, Zhang J, Su Y, Li Q, Yuan J, Liu L, Moreno-De-Luca A, MacLennan AH, Gecz J, Zhu D, Wang X, Zhu C, Xing Q. Wang Y, et al. Among authors: maclennan ah. Nat Med. 2024 May;30(5):1395-1405. doi: 10.1038/s41591-024-02912-z. Epub 2024 May 1. Nat Med. 2024. PMID: 38693247
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics; Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study; Hedrich UBS, Scheffer IE, Helbig I… See abstract for full author list ➔ Helbig KL, et al. Among authors: maclennan ah. Am J Hum Genet. 2018 Nov 1;103(5):666-678. doi: 10.1016/j.ajhg.2018.09.006. Epub 2018 Oct 18. Am J Hum Genet. 2018. PMID: 30343943 Free PMC article.
Reply.
Maclennan AH, Thompson SC, Gecz J. Maclennan AH, et al. Am J Obstet Gynecol. 2016 May;214(5):671. doi: 10.1016/j.ajog.2016.01.179. Epub 2016 Jan 29. Am J Obstet Gynecol. 2016. PMID: 26829505 No abstract available.
Relaxin--a review.
MacLennan AH. MacLennan AH. Aust N Z J Obstet Gynaecol. 1981 Nov;21(4):195-202. doi: 10.1111/j.1479-828x.1981.tb00130.x. Aust N Z J Obstet Gynaecol. 1981. PMID: 6280666 Review.
Oral contraceptives.
Maclennan AH. Maclennan AH. Curr Ther (Seaforth). 1987 Dec;28(12):113-22. Curr Ther (Seaforth). 1987. PMID: 12317413
The weight problem.
Sturdee DW, MacLennan AH. Sturdee DW, et al. Among authors: maclennan ah. Climacteric. 2007 Apr;10(2):83-4. doi: 10.1080/13697130701276053. Climacteric. 2007. PMID: 17453855 No abstract available.
WHI, WHI, WHI?
MacLennan AH, Sturdee DW. MacLennan AH, et al. Climacteric. 2004 Sep;7(3):221-4. doi: 10.1080/13697130400001331. Climacteric. 2004. PMID: 15669545 No abstract available.
The genetic basis of cerebral palsy.
Fahey MC, Maclennan AH, Kretzschmar D, Gecz J, Kruer MC. Fahey MC, et al. Among authors: maclennan ah. Dev Med Child Neurol. 2017 May;59(5):462-469. doi: 10.1111/dmcn.13363. Epub 2017 Jan 1. Dev Med Child Neurol. 2017. PMID: 28042670 Free article. Review.
189 results