Talebizadeh, Zohreh : rechercher sur Z-Library

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1

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

Zohreh Talebizadeh, Philip M. Kelley, James W. Askew, Kirk W. Beisel, Shelley D. Smith

Journal:

Année:

1999

Langue:

english

Fichier:

PDF, 407 KB

english, 1999

2

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

Merlin G. Butler, Mariana F. Theodoro, Douglas C. Bittel, Paul J. Kuipers, Daniel J. Driscoll, Zohreh Talebizadeh

Journal:

American Journal of Medical Genetics Part A

Année:

2007

Langue:

english

Fichier:

PDF, 139 KB

english, 2007

3

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

Bing Han, Xue-wen Chen, Zohreh Talebizadeh

Journal:

BMC Bioinformatics

Année:

2011

Langue:

english

Fichier:

PDF, 301 KB

english, 2011

4

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

Gregory Matuszek, Zohreh Talebizadeh

Journal:

BMC Medical Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 1.62 MB

english, 2009

5

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

Zohreh Talebizadeh, Douglas C. Bittel, Olivia J. Veatch, Merlin G. Butler, T. Nicole Takahashi, Judith H. Miles, Ching H. Wang

Journal:

Journal of Autism and Developmental Disorders

Année:

2004

Langue:

english

Fichier:

PDF, 59 KB

english, 2004

6

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

Mariana F. Theodoro, Zohreh Talebizadeh, Merlin G. Butler

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 143 KB

english, 2006

7

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

Zohreh Talebizadeh, Merlin G. Butler, Mariana F. Theodoro

Journal:

Autism Research

Année:

2008

Langue:

english

Fichier:

PDF, 35 KB

english, 2008

8

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

Zohreh Talebizadeh, Merlin G. Butler, Mariana F. Theodoro

Journal:

Autism Research

Année:

2008

Langue:

english

Fichier:

PDF, 324 KB

english, 2008

9

Regulation of Gene Expression by Small RNAs

Zohreh Talebizadeh

Journal:

The American Journal of Human Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 55 KB

english, 2010

10

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

Peter S. Bazeley, Valery Shepelev, Zohreh Talebizadeh, Merlin G. Butler, Larisa Fedorova, Vadim Filatov, Alexei Fedorov

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 506 KB

english, 2008

11

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

Douglas C. Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, Daniel J. Driscoll, Merlin G. Butler

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 349 KB

english, 2005

12

X chromosome gene expression in human tissues: Male and female comparisons

Zohreh Talebizadeh, Stephen D. Simon, Merlin G. Butler

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 688 KB

english, 2006

13

Genetic studies of complex human diseases: Characterizing SNP-disease associations using Bayesian networks

Bing Han, Xue-wen Chen, Zohreh Talebizadeh, Hua Xu

Journal:

BMC Systems Biology

Année:

2012

Langue:

english

Fichier:

PDF, 1.19 MB

english, 2012

14

A proof-of-concept study

Talebizadeh, Zohreh, Aldenderfer, Richard, Wen Chen, Xue

Journal:

Psychiatric Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 502 KB

english, 2014

15

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

Talebizadeh, Zohreh, Kibiryeva, Nataliya, Bittel, Douglas, Butler, Merlin

Journal:

International Journal of Molecular Medicine

Année:

2005

Langue:

english

Fichier:

PDF, 2.78 MB

english, 2005

16

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

Talebizadeh, Zohreh, Shah, Ayten

Journal:

The Patient: Patient-Centered Outcomes Research

Année:

2018

Langue:

english

Fichier:

PDF, 988 KB

english, 2018

17

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

Booth, Kevin T., Askew, James W., Talebizadeh, Zohreh, Huygen, Patrick L. M., Eudy, James, Kenyon, Judith, Hoover, Denise, Hildebrand, Michael S., Smith, Katherine R., Bahlo, Melanie, Kimberling, Will

Journal:

Genetics in Medicine

Année:

2018

Langue:

english

Fichier:

PDF, 937 KB

english, 2018

18

Lessons learned from the DFNA37 gene discovery odyssey

Talebizadeh, Zohreh

Journal:

Genetics in Medicine

Année:

2018

Langue:

english

Fichier:

PDF, 202 KB

english, 2018

19

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

Talebizadeh, Zohreh, Shah, Ayten, DiTacchio, Luciano

Journal:

Autism Research

Année:

2019

Langue:

english

Fichier:

PDF, 2.23 MB

english, 2019

20

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

Talebizadeh, Zohreh, Shah, Ayten, DiTacchio, Luciano

Journal:

Autism Research

Année:

2019

Fichier:

PDF, 2.23 MB

2019

21

The AutGO Initiative: A Conceptual Framework for Developing GeneticsâOutcomes Research Hypotheses

Talebizadeh, Zohreh, Shah, Ayten

Journal:

Autism Research

Année:

2020

Fichier:

PDF, 920 KB

2020