Z. Talebizadeh

发表

Integrating P-values for Genetic and Genomic Data Analysis

R. Charnigo, Hongying Dai, S. Ye, 2012 .

Comparison of X-chromosome inactivation patterns in multiple tissues from human females

Z. Talebizadeh, M. Theodoro, M. Butler, 2007, Journal of Medical Genetics.

Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

J. W. Askew, Katherine R. Smith, M. Bahlo, 2018, Genetics in Medicine.

Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region

Z. Talebizadeh, M. Butler, D. Bittel, 2002, Journal of medical genetics.

Insulin resistance and obesity‐related factors in Prader–Willi syndrome: Comparison with obese subjects

Z. Talebizadeh, M. Butler, 2004, Clinical genetics.

The Impact of Integrative Unconventional Data Analysis Approaches on Advancing Autism Genetics Research

Z. Talebizadeh, Ayten Shah, 2014 .

Plasma Peptide YY and Ghrelin Levels in Infants and Children with Prader-Willi Syndrome

Z. Talebizadeh, M. Butler, D. Bittel, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Body Composition and Fatness Patterns in Prader‐Willi Syndrome: Comparison with Simple Obesity

Z. Talebizadeh, M. Theodoro, M. Butler, 2006, Obesity.

A proof-of-concept study: exon-level expression profiling and alternative splicing in autism using lymphoblastoid cell lines

Z. Talebizadeh, Richard Aldenderfer, Xue Wen Chen, 2014, Psychiatric genetics.

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

Z. Talebizadeh, M. Theodoro, M. Butler, 2005, Journal of Medical Genetics.

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

C Eng, J H Miles, C. Eng, 2005, Journal of Medical Genetics.

Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism

Z. Talebizadeh, M. Theodoro, M. Butler, 2008, Autism research : official journal of the International Society for Autism Research.

Prader-Willi syndrome and a deletion / duplication within the 15 q 11-q 13 region

Z. Talebizadeh, M. Butler, D. Bittel, 2002 .

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

J. W. Askew, K. Beisel, Z. Talebizadeh, 1999, Human mutation.

The potential role of a retrotransposed gene and a long noncoding RNA in regulating an X‐linked chromatin gene (KDM5C): Novel epigenetic mechanism in autism

Z. Talebizadeh, Luciano DiTacchio, Ayten Shah, 2019, Autism research : official journal of the International Society for Autism Research.

A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism

Zohreh Talebizadeh, D. Arking, Z. Talebizadeh, 2013, PloS one.

microRNAs and Gene–Environment Interactions in Autism: Effects of Prenatal Maternal Stress and the SERT Gene on Maternal microRNA Expression

Bradley J. Ferguson, Patrick M. Hecht, D. Beversdorf, 2021, Frontiers in Psychiatry.

Letter to the Editor: Do Known Mutations in Neuroligin Genes (NLGN3 and NLGN4) Cause Autism?

Z. Talebizadeh, Ching H. Wang, M. Butler, 2004, Journal of autism and developmental disorders.

No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)

Z. Talebizadeh, M. Butler, J. Miles, 2002, Journal of medical genetics.

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.

Z. Talebizadeh, M. Butler, D. Bittel, 2004, Pediatrics.

FEPI-MB: identifying SNPs-disease association using a Markov Blanket-based approach

Xue-wen Chen, Bing Han, Zohreh Talebizadeh, 2011, BMC Bioinformatics.

Autism genetic database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites

Zohreh Talebizadeh, Z. Talebizadeh, Gregory Matuszek, 2009, BMC Medical Genetics.

X‐chromosome inactivation patterns in females with Prader–Willi syndrome

D. J. Driscoll, Z. Talebizadeh, M. Theodoro, 2007, American journal of medical genetics. Part A.

Brief Report: Non-Random X Chromosome Inactivation in Females with Autism

Z. Talebizadeh, M. Butler, D. Bittel, 2005, Journal of autism and developmental disorders.

X chromosome gene expression in human tissues: male and female comparisons.

Zohreh Talebizadeh, Z. Talebizadeh, M. Butler, 2006, Genomics.

snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions.

Valery Shepelev, Alexei Fedorov, Zohreh Talebizadeh, 2008, Gene.

DFNA2/KCNQ4 and its manifestations.

C. Cremers, Z. Talebizadeh, F. Declau, 2002, Advances in oto-rhino-laryngology.

The AutGO Initiative: A Conceptual Framework for Developing Genetics‐Outcomes Research Hypotheses

Z. Talebizadeh, Ayten Shah, 2020, Autism research : official journal of the International Society for Autism Research.

Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

Z. Talebizadeh, M. Butler, D. Bittel, 2003, Journal of medical genetics.

Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndrome.

Z. Talebizadeh, M. Butler, D. Bittel, 2005, International journal of molecular medicine.

Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism

Z. Talebizadeh, M. Theodoro, M. Butler, 2008 .

Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.

D. J. Driscoll, Z. Talebizadeh, M. Butler, 2005, Genomics.

Regulation of Gene Expression by Small RNAs

Z. Talebizadeh, 2010 .

The Relationship between Maternal Antibodies to Fetal Brain and Prenatal Stress Exposure in Autism Spectrum Disorder

Bradley J. Ferguson, Patrick M. Hecht, D. Beversdorf, 2023, Metabolites.

Building a Bridge Between Genetics and Outcomes Research: Application in Autism (The AutGO Study)

H. Saiedian, J. Spertus, Leon Rozenblit, 2018, The Patient - Patient-Centered Outcomes Research.

or Type II Deletion and Maternal Disomy Behavioral Differences Among Subjects With Prader-Willi Syndrome and Type I

Z. Talebizadeh, M. Butler, D. Bittel, 2007 .

ATM mutations in Finnish breast cancer patients

A. Børresen-Dale, R. Winqvist, Z. Talebizadeh, 2002, Journal of medical genetics.

X‐chromosome inactivation patterns in females with Prader–Willi syndrome

D. J. Driscoll, Z. Talebizadeh, M. Theodoro, 2007, American journal of medical genetics. Part A.

microRNA as a Maternal Marker for Prenatal Stress-Associated ASD, Evidence from a Murine Model

Z. Talebizadeh, N. Kibiryeva, Matt J. Will, 2023, Journal of personalized medicine.

patterns in multiple tissues from human females Comparison of X-chromosome inactivation

Z. Talebizadeh, M. Theodoro, M. Butler, 2008 .

Developing a community-led rare disease ELSI research agenda

Z. Talebizadeh, Courtney Berrios, Macy McBeth, 2024, Orphanet journal of rare diseases.