S. Kisselev

发表

Candidate Sequence Variants and Fetal Hemoglobin in Children with Sickle Cell Disease Treated with Hydroxyurea

K. Neville, L. Clark, S. Barral, 2013, PloS one.

Olfaction in Parkin heterozygotes and compound heterozygotes

K. Marder, M. Rezak, L. Cote, 2010, Neurology.

Acute Kidney Injury Due to Collapsing Glomerulopathy Following COVID-19 Infection

V. D’Agati, T. Nickolas, A. Gharavi, 2020, Kidney International Reports.

COVID-19-Associated Glomerular Disease.

A. Gharavi, Aneesha Shetty, S. Quaggin, 2020, Journal of the American Society of Nephrology : JASN.

Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor.

N. Park, Joseph H. Lee, E. Louis, 2010, Parkinsonism & related disorders.

Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease

K. Marder, R. Mayeux, N. Park, 2015, PloS one.

Candidate genes for Alzheimer's disease are associated with individual differences in plasma levels of beta amyloid peptides in adults with Down syndrome

B. Tycko, N. Park, N. Schupf, 2015, Neurobiology of Aging.

Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population

Karen Marder, Stanley Fahn, Andrew Browne, 2011, BMC Medical Genetics.

Identification of candidate genes for familial early-onset essential tremor

I. Ionita-Laza, A. Floratos, E. Louis, 2015, European Journal of Human Genetics.

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.

T. Palomero, V. D’Agati, H. Kim, 2011, Kidney international.

Genetic analysis of the FUS/TLS gene in essential tremor

E. Louis, G. Rouleau, L. Clark, 2013, European journal of neurology.

Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.

K. Marder, M. Rezak, L. Cote, 2010, Archives of neurology.

Promoter methylation‐mediated inactivation of PCDH10 in acute lymphoblastic leukemia contributes to chemotherapy resistance

G. Bhagat, L. Clark, A. Freddy, 2011, Genes, chromosomes & cancer.

Cognitive performance of GBA mutation carriers with early-onset PD

K. Marder, M. Rezak, L. Cote, 2012, Neurology.

Prediction of disability-free survival in healthy older people

Michael S. Warren, H. C. Siew, Suzanne G. Orchard, 2022, GeroScience.

PCDH10 promoter hypermethylation is frequent in most histologic subtypes of mature lymphoid malignancies and occurs early in lymphomagenesis

B. Tycko, G. Bhagat, L. Clark, 2013, Genes, chromosomes & cancer.

Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.

K. Marder, M. Rezak, L. Cote, 2010, Archives of neurology.

Replication of the LINGO1 gene association with essential tremor in a North American population

N. Park, Joseph H. Lee, E. Louis, 2010, European Journal of Human Genetics.

Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews

K. Marder, L. Cote, S. Fahn, 2013, Molecular genetics & genomic medicine.

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease.

K. Marder, M. Rezak, L. Cote, 2009, Archives of neurology.

Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study

K. Marder, M. Rezak, L. Cote, 2010, Journal of the International Neuropsychological Society.

Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

K. Marder, M. Rezak, L. Cote, 2010, Journal of clinical and experimental neuropsychology.

Association of glucocerebrosidase mutations with dementia with lewy bodies.

K. Marder, R. Mayeux, L. Cote, 2009, Archives of neurology.

Candidate gene analysis for Alzheimer's disease in adults with Down syndrome

B. Tycko, N. Schupf, J. Luchsinger, 2017, Neurobiology of Aging.

Distribution of mononucleotide repeats in bacterial chromosomes: A/T-tracts dominate on G/C-tracts

V. M. Komarov, O. Ozoline, S. Kisselev, 2010 .

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease.

K. Marder, M. Rezak, L. Cote, 2009, Archives of neurology.

Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.

K. Marder, M. Rezak, L. Cote, 2010, Archives of neurology.