S. Singh

发表

CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene

C. Scriver, B. Murphy, S. Singh, 2006, Human mutation.

Distribution and molecular characterization of mRNA-binding proteins specific to the (U)15 region of 3' UTR of the mouse catalase (Cas-1).

S. Singh, X. Song, 2001, DNA and cell biology.

Post-zygotic genomic changes in glutamate and dopamine pathway genes may explain discordance of monozygotic twins for schizophrenia

Shiva M. Singh, C. Castellani, M. G. Melka, 2017, Clinical and Translational Medicine.

A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.

J. Jung, P. Ainsworth, D. Rodenhiser, 1993, Journal of medical genetics.

A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkage.

J. Jung, D. Rodenhiser, M. Coulter-Mackie, 1991, Journal of medical genetics.

Appraisal of genetic and epigenetic congruity of a monozygotic twin pair discordant for schizophrenia

R. O'Reilly, B. Murphy, S. Singh, 2003, Journal of medical genetics.

Site and sequence specific DNA methylation in the neurofibromatosis (NF1) gene includes C5839T: the site of the recurrent substitution mutation in exon 31.

D. Rodenhiser, J. Andrews, S. Singh, 1996, Human molecular genetics.

DQB1-0602 (DQw1) is not present in most nonDR2 Caucasian narcoleptics.

C. Guilleminault, E. Mignot, W. Dement, 1992, Sleep.

Complementary approaches involving monozygotic twins and single neuron genomics support postzygotic somatic mutations in schizophrenia

C. Castellani, S. Singh, P. W. Win, 2022, Schizophrenia Research.

Evaluation of serum-associated embryotoxicity/mutagenicity in females with reproductive dysfunctions using preimplantation mouse embryos in vitro.

J. Jung, S. Singh, A. Porter, 1988, Mutagenesis.

Evidence of DNA methylation in the neurofibromatosis type 1 (NF1) gene region of 17q11.2.

D. Rodenhiser, M. Coulter-Mackie, S. Singh, 1993, Human molecular genetics.

Copy number variation showers in schizophrenia: an emerging hypothesis

C. Castellani, R. O'Reilly, S. Singh, 2009, Molecular Psychiatry.

Molecular characterization of a MSRV-like sequence identified by RDA from monozygotic twin pairs discordant for schizophrenia.

E. Torrey, T. Klempan, R. O'Reilly, 1999, Genomics.

Retroviruses and schizophrenia revisited.

R. O'Reilly, S. Singh, 1996, American journal of medical genetics.

Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene.

J. Jung, D. Rodenhiser, J. Andrews, 1997, Mutation research.

Strategies and applications of DNA level diagnosis in genetic diseases: past experiences and future directions.

J. Jung, P. Ainsworth, Shiva M. Singh, 1996, Biotechnology annual review.

Monozygotic twins with chromosome 22q11 deletion and discordant phenotypes: updates with an epigenetic hypothesis

R. O'Reilly, B. Murphy, S. Singh, 2002, Journal of Medical Genetics.

Search for retroviral related DNA polymorphisms using RAPD PCR in schizophrenia.

T. Klempan, R. O'Reilly, S. Singh, 1999, Biochimica et biophysica acta.

Integration of DNA sequence and DNA methylation changes in monozygotic twin pairs discordant for schizophrenia

C. Castellani, M. G. Melka, R. O'Reilly, 2015, Schizophrenia Research.

IgH (μ-switch and γ-1) region restriction fragment length polymorphism in human narcolepsy

C. Guilleminault, E. Mignot, W. Dement, 1996, Journal of Clinical Immunology.

A single-primer PCR-based retroviral-related DNA polymorphism shared by two distinct human populations.

T. Klempan, R. O'Reilly, S. Singh, 1998, Genome.

The evolution of species-type specificity in the global DNA sequence organization of mitochondrial genomes.

K A Hill, K. Hill, S M Singh, 1997, Genome.

The profile and distribution of skin disorders in ambulatory community-dwelling adult patients with Schizophrenia: a study from North India

T. Narang, S. Singh, S. Kathiravan, 2022, medRxiv.