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

Year Number of Results
1981 1
1983 2
1984 1
1985 1
1986 1
1987 1
1989 4
1990 2
1991 4
1992 2
1993 2
1994 1
1995 1
1996 3
1997 5
1998 3
1999 5
2000 7
2001 2
2002 1
2003 3
2004 6
2005 4
2006 6
2007 4
2008 5
2009 4
2010 3
2011 2
2012 1
2013 2
2014 4
2015 5
2016 6
2017 3
2018 2
2019 1
2020 1
2021 1
2022 3
2023 5
2024 1

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116 results

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Page 1
Postinfectious Inflammation, Autoimmunity, and Obsessive-Compulsive Disorder: Sydenham Chorea, Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infection, and Pediatric Acute-Onset Neuropsychiatric Disorder.
Vreeland A, Calaprice D, Or-Geva N, Frye RE, Agalliu D, Lachman HM, Pittenger C, Pallanti S, Williams K, Ma M, Thienemann M, Gagliano A, Mellins E, Frankovich J. Vreeland A, et al. Among authors: lachman hm. Dev Neurosci. 2023;45(6):361-374. doi: 10.1159/000534261. Epub 2023 Sep 22. Dev Neurosci. 2023. PMID: 37742615 Free article. Review.
Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.
Wojcik MH, Srivastava S, Agrawal PB, Balci TB, Callewaert B, Calvo PL, Carli D, Caudle M, Colaiacovo S, Cross L, Demetriou K, Drazba K, Dutra-Clarke M, Edwards M, Genetti CA, Grange DK, Hickey SE, Isidor B, Küry S, Lachman HM, Lavillaureix A, Lyons MJ, Marcelis C, Marco EJ, Martinez-Agosto JA, Nowak C, Pizzol A, Planes M, Prijoles EJ, Riberi E, Rush ET, Russell BE, Sachdev R, Schmalz B, Shears D, Stevenson DA, Wilson K, Jansen S, de Vries BBA, Curry CJ. Wojcik MH, et al. Among authors: lachman hm. Am J Med Genet A. 2023 Jul;191(7):1900-1910. doi: 10.1002/ajmg.a.63226. Epub 2023 May 14. Am J Med Genet A. 2023. PMID: 37183572
Identification of ultra-rare genetic variants in pediatric acute onset neuropsychiatric syndrome (PANS) by exome and whole genome sequencing.
Trifiletti R, Lachman HM, Manusama O, Zheng D, Spalice A, Chiurazzi P, Schornagel A, Serban AM, van Wijck R, Cunningham JL, Swagemakers S, van der Spek PJ. Trifiletti R, et al. Among authors: lachman hm. Sci Rep. 2022 Jun 30;12(1):11106. doi: 10.1038/s41598-022-15279-3. Sci Rep. 2022. PMID: 35773312 Free PMC article.
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Lin JR, Zhao Y, Jabalameli MR, Nguyen N, Mitra J; International 22q11.DS Brain and Behavior Consortium; Swillen A, Vorstman JAS, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Owen MJ, Williams NM, Bassett AS, McDonald-McGinn DM, Gur RE, Bearden CE, Morrow BE, Lachman HM, Zhang ZD. Lin JR, et al. Among authors: lachman hm. Mol Psychiatry. 2023 May;28(5):2071-2080. doi: 10.1038/s41380-023-02009-y. Epub 2023 Mar 3. Mol Psychiatry. 2023. PMID: 36869225
116 results