Projects per year
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Dive into the research topics where William Johnson is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Projects
- 2 Finished
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New DHFR Deletion Polymorphism - A Risk Factor for SB?
National Institute of Neurological Disorders and Stroke
9/15/02 → 6/30/05
Project: Research project
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HEX DEFICIENIES: BIOCHEMICAL &MOLECULAR GENETICS
National Institute of Neurological Disorders and Stroke
1/1/90 → 1/1/90
Project: Research project
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Disorders of glycoprotein degradation: sialidosis, fucosidosis, α-mannosidosis, β-mannosidosis, and aspartylglycosaminuria
Johnson, W. G., Jan 1 2020, Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease: Volume 1. Elsevier, p. 519-534 16 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
1 Scopus citations -
β-Galactosidase deficiency: GM1 gangliosidosis, Morquio B disease, and galactosialidosis
Johnson, W. G., Jan 1 2020, Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease: Volume 1. Elsevier, p. 535-546 12 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
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Clinical-genetic associations in the Prospective Huntington at Risk Observational Study (PHAROS) implications for clinical trials
The Huntington Study Group PHAROS Investigators, Jan 2016, In: JAMA Neurology. 73, 1, p. 102-110 9 p.Research output: Contribution to journal › Article › peer-review
Open Access30 Scopus citations -
A GLUTATHIONE S-TRANSFEREASE P1 HAPLOTYPE ACTING IN MOTHERS DURING PREGNANCY MAY INCREASE RISK OF AUTISTIC DISORDER IN HER AFFECTED OFFSPRING
Johnson, W. & Stenroos, E., Mar 2014Research output: Innovation
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ASSOCIATION OF GSTM1 WITH AUTISM AND ASSAYS AND METHODS BASED THEREON
Johnson, W., Buyske, S., Lambert, G., Ming, S., Mars, A., Stenroos, E. & Williams, T., Mar 2014Research output: Innovation