Jennifer Reichert
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Explore the profile of Jennifer Reichert including associated specialties, affiliations and a list of published articles.
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9
Citations
3526
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Recent Articles
1.
Satterstrom F, Kosmicki J, Wang J, Breen M, De Rubeis S, An J, et al.
Cell
. 2020 Jan;
180(3):568-584.e23.
PMID: 31981491
We present the largest exome sequencing study of autism spectrum disorder (ASD) to date (n = 35,584 total samples, 11,986 with ASD). Using an enhanced analytical framework to integrate de...
2.
Mahjani B, Dellenvall K, Grahnat A, Karlsson G, Tuuliainen A, Reichert J, et al.
Soc Psychiatry Psychiatr Epidemiol
. 2020 Jan;
55(10):1383-1393.
PMID: 31907560
Purpose: The EGOS study (Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden) is a large-scale, epidemiological, prospective cohort that is used to identify genetic and environmental...
3.
Grove J, Ripke S, Als T, Mattheisen M, Walters R, Won H, et al.
Nat Genet
. 2019 Feb;
51(3):431-444.
PMID: 30804558
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but...
4.
Barbosa M, Joshi R, Garg P, Martin-Trujillo A, Patel N, Jadhav B, et al.
Nat Commun
. 2018 May;
9(1):2064.
PMID: 29802345
Certain human traits such as neurodevelopmental disorders (NDs) and congenital anomalies (CAs) are believed to be primarily genetic in origin. However, even after whole-genome sequencing (WGS), a substantial fraction of...
5.
Gaugler T, Klei L, Sanders S, Bodea C, Goldberg A, Lee A, et al.
Nat Genet
. 2014 Jul;
46(8):881-5.
PMID: 25038753
A key component of genetic architecture is the allelic spectrum influencing trait variability. For autism spectrum disorder (herein termed autism), the nature of the allelic spectrum is uncertain. Individual risk-associated...
6.
Glessner J, Wang K, Cai G, Korvatska O, Kim C, Wood S, et al.
Nature
. 2009 May;
459(7246):569-73.
PMID: 19404257
Autism spectrum disorders (ASDs) are childhood neurodevelopmental disorders with complex genetic origins. Previous studies focusing on candidate genes or genomic regions have identified several copy number variations (CNVs) that are...
7.
Sakurai T, Reichert J, Hoffman E, Cai G, Jones H, Faham M, et al.
Autism Res
. 2009 Apr;
1(4):251-7.
PMID: 19360675
In the current study we explored the hypothesis that rare variants in SLC6A4 contribute to autism susceptibility and to rigid-compulsive behaviors in autism. We made use of a large number...
8.
Buxbaum J, Cai G, Chaste P, Nygren G, Goldsmith J, Reichert J, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2007 Apr;
144B(4):484-91.
PMID: 17427195
Mutations in the PTEN gene are associated with a broad spectrum of disorders, including Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome, and Lhermitte-Duclos disease. In addition, PTEN mutations have been...
9.
Faham M, Zheng J, Moorhead M, Fakhrai-Rad H, Namsaraev E, Wong K, et al.
Proc Natl Acad Sci U S A
. 2005 Oct;
102(41):14717-22.
PMID: 16203980
Identification of the genetic basis of common disease may require comprehensive sequence analysis of coding regions and regulatory elements in patients and controls to find genetic effects caused by rare...