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Biochemical and Biophysical Research Communications|July 2, 1998
Structural characterization and mapping of the normal epithelial cell-specific 1 geneL Luo, J A Herbrick, S W Scherer, et al.
Genome Biology|September 12, 2025
Diverse short tandem repeat sequences influence gene regulation in human populationsAleksandra Mitina, Worrawat Engchuan, Brett Trost, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autismJohn B Vincent, Sandy Thevarkunnel, Debbie Kolozsvari, et al.
BMC Bioinformatics|May 27, 2011
A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV dataTakeshi Nishiyama, Kunihiko Takahashi, Toshiro Tango, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1993
Mapping the midkine family of developmentally regulated signaling moleculesC L Peichel, S W Scherer, L C Tsui, et al.
American Journal of Medical Genetics|January 31, 1997
Physical mapping of the chromosome 7 breakpoint region in an SLOS patient with t(7;20) (q32.1;q13.2)T L Alley, S W Scherer, J J Huizenga, et al.
Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Genomics|November 15, 2001
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31J Cheung, E Petek, K Nakabayashi, et al.
Pediatric Research|June 18, 2009
Whole genome scanning: resolving clinical diagnosis and management amidst complex dataSarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, et al.
BMC Medical Genomics|March 19, 2015
Performance of case-control rare copy number variation annotation in classification of autismWorrawat Engchuan, Kiret Dhindsa, Anath C Lionel, et al.
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