Liu X - Search Results

1

Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.

Heidari A, Tongsook C, Najafipour R, Musante L, Vasli N, Garshasbi M, Hu H, Mittal K, McNaughton AJ, Sritharan K, Hudson M, Stehr H, Talebi S, Moradi M, Darvish H, Arshad Rafiq M, Mozhdehipanah H, Rashidinejad A, Samiei S, Ghadami M, Windpassinger C, Gillessen-Kaesbach G, Tzschach A, Ahmed I, Mikhailov A, Stavropoulos DJ, Carter MT, Keshavarz S, Ayub M, Najmabadi H, Liu X, Ropers HH, Macheroux P, Vincent JB. Heidari A, et al. Among authors: liu x. Hum Mol Genet. 2015 Oct 15;24(20):5697-710. doi: 10.1093/hmg/ddv286. Epub 2015 Jul 23. Hum Mol Genet. 2015. PMID: 26206890 Free PMC article.

2

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.

Liu X, Novosedlik N, Wang A, Hudson ML, Cohen IL, Chudley AE, Forster-Gibson CJ, Lewis SM, Holden JJ. Liu X, et al. Eur J Hum Genet. 2009 Feb;17(2):228-35. doi: 10.1038/ejhg.2008.148. Epub 2008 Aug 27. Eur J Hum Genet. 2009. PMID: 18728693 Free PMC article.

3

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.

Qiao Y, Harvard C, Tyson C, Liu X, Fawcett C, Pavlidis P, Holden JJ, Lewis ME, Rajcan-Separovic E. Qiao Y, et al. Among authors: liu x. Hum Genet. 2010 Aug;128(2):179-94. doi: 10.1007/s00439-010-0837-0. Epub 2010 May 29. Hum Genet. 2010. PMID: 20512354

4

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.

Liu X, Malenfant P, Reesor C, Lee A, Hudson ML, Harvard C, Qiao Y, Persico AM, Cohen IL, Chudley AE, Forster-Gibson C, Rajcan-Separovic E, Lewis ME, Holden JJ. Liu X, et al. Eur J Hum Genet. 2011 Dec;19(12):1264-70. doi: 10.1038/ejhg.2011.112. Epub 2011 Jul 13. Eur J Hum Genet. 2011. PMID: 21750575 Free PMC article.

5

DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families.

Hettinger JA, Liu X, Hudson ML, Lee A, Cohen IL, Michaelis RC, Schwartz CE, Lewis SM, Holden JJ. Hettinger JA, et al. Among authors: liu x. Behav Brain Funct. 2012 May 4;8:19. doi: 10.1186/1744-9081-8-19. Behav Brain Funct. 2012. PMID: 22559203 Free PMC article.

6

Behavioral development and sociodemographics of infants and young children at higher and lower risk for autism spectrum disorders.

Feldman MA, Hendry AM, Ward RA, Hudson M, Liu X. Feldman MA, et al. Among authors: liu x. J Autism Dev Disord. 2015 May;45(5):1167-75. doi: 10.1007/s10803-014-2277-5. J Autism Dev Disord. 2015. PMID: 25326257

7

Interplay between maternal Slc6a4 mutation and prenatal stress: a possible mechanism for autistic behavior development.

Sjaarda CP, Hecht P, McNaughton AJM, Zhou A, Hudson ML, Will MJ, Smith G, Ayub M, Liang P, Chen N, Beversdorf D, Liu X. Sjaarda CP, et al. Among authors: liu x. Sci Rep. 2017 Aug 18;7(1):8735. doi: 10.1038/s41598-017-07405-3. Sci Rep. 2017. PMID: 28821725 Free PMC article.

8

Comorbid and inflammatory characteristics of genetic subtypes of clonal hematopoiesis.

Cook EK, Izukawa T, Young S, Rosen G, Jamali M, Zhang L, Johnson D, Bain E, Hilland J, Ferrone CK, Buckstein J, Francis J, Momtaz B, McNaughton AJM, Liu X, Snetsinger B, Buckstein R, Rauh MJ. Cook EK, et al. Among authors: liu x. Blood Adv. 2019 Aug 27;3(16):2482-2486. doi: 10.1182/bloodadvances.2018024729. Blood Adv. 2019. PMID: 31434682 Free PMC article.

9

Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism.

Sjaarda CP, Wood S, McNaughton AJM, Taylor S, Hudson ML, Liu X, Guerin A, Ayub M. Sjaarda CP, et al. Among authors: liu x. J Hum Genet. 2020 Mar;65(3):287-296. doi: 10.1038/s10038-019-0707-0. Epub 2019 Dec 12. J Hum Genet. 2020. PMID: 31827253

10

De novo duplication on Chromosome 19 observed in nuclear family displaying neurodevelopmental disorders.

Sjaarda CP, Kaiser B, McNaughton AJM, Hudson ML, Harris-Lowe L, Lou K, Guerin A, Ayub M, Liu X. Sjaarda CP, et al. Among authors: liu x. Cold Spring Harb Mol Case Stud. 2020 Jun 12;6(3):a004721. doi: 10.1101/mcs.a004721. Print 2020 Jun. Cold Spring Harb Mol Case Stud. 2020. PMID: 32321736 Free PMC article.

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