Wolfe, Lynne
National Institutes of Health · National Human Genome Research Institute
6 papers on CoChatORCID 0000-0001-7628-5741
Most cited papers
- Verified
Diagnosis and management of mitochondrial disease: a consensus statement from the mitochondrial medicine society
Parikh, S., Goldstein, A., Koenig, M. K., Scaglia, F., Enns, G. M., Saneto, R., Anselm, I., Cohen, B. H., Falk, M. J., Greene, C., et al. (2015) · Genetics in Medicine
Mitochondrial Function and PathologyMetabolism and Genetic Disorders
Cited by 607
- Verified
The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases
Gahl, W. A., Markello, T. C., Toro, C., Fajardo, K. F., Sincan, M., Gill, F., Carlson-Donohoe, H., Gropman, A., Pierson, T. M., Golas, G., et al. (2012) · Genetics in Medicine
Genomics and Rare DiseasesMetabolism and Genetic Disorders
Cited by 291
- Verified
Nutritional interventions in primary mitochondrial disorders: Developing an evidence base
Camp, K. M., Krotoski, D., Parisi, M. A., Gwinn, K. A., Cohen, B. H., Cox, C. S., Enns, G. M., Falk, M. J., Goldstein, A. C., Gopal-Srivastava, R., et al. (2016) · Molecular Genetics and Metabolism
Metabolism and Genetic DisordersMitochondrial Function and Pathology
Cited by 59
- Verified
Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases
Kobren, S. N., Baldridge, D., Velinder, M., Krier, J. B., LeBlanc, K., Esteves, C., Pusey, B. N., Züchner, S., Blue, E., Lee, H., et al. (2021) · Genetics in Medicine
Genomics and Rare DiseasesGenomics and Phylogenetic Studies
Cited by 27
- Verified
Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies
Küry, S., Stanton, J. E., van Woerden, G., Hsieh, T.-C., Rosenfelt, C., Scott-Boyer, M. P., Most, V., Wang, T., Papendorf, J. J., de Konink, C., et al. (2024) · medRxiv
Genetics and Neurodevelopmental DisordersUbiquitin and proteasome pathways
Cited by 6
- Verified
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies
Küry, S., Stanton, J. E., van Woerden, G. M., Bosc-Rosati, A., Hsieh, T.-C., Bray, L., Oloudé, M., Rosenfelt, C., Scott-Boyer, M. P., Most, V., et al. (2025) · Nature Communications
Ubiquitin and proteasome pathwaysGenetics and Neurodevelopmental Disorders
Cited by 3
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