E-LIB Suche - Ergebnisse für: Zahir, Farah R.

1

Methionine Is a Major Methyl Donor Whose Dietary Intake Lik..:

, In: Nutritional Neurosciences; Proteins Associated with Neurodevelopmental Disorders,

Mubarak, Ghada ; Zahir, Farah R. - p. 117-134 , 2022

Link: https://doi.org/10.1007/..

2

Recent Major Transcriptomics and Epitranscriptomics Contrib..:

Mubarak, Ghada ; Zahir, Farah R.
Journal of Personalized Medicine. 12 (2022) 2 - p. 199 , 2022

Link: https://doi.org/10.3390/..

3

Editorial on the Paper "The Epidemiology and Genetics of Hy..:

Zahir, Farah R.
Journal of Personalized Medicine. 12 (2022) 8 - p. 1331 , 2022

Link: https://doi.org/10.3390/..

4

The Need for Precision Therapies as Determined by Genetic S..:

Zahir, Farah R.
Journal of Personalized Medicine. 11 (2021) 12 - p. 1353 , 2021

Link: https://doi.org/10.3390/..

5

First Whole Transcriptome RNAseq on CHD8 Haploinsufficient ..:

Yasin, Heba ; Stowe, Robert ; Wong, Chi Kin..
Cureus. , 2020

Link: https://doi.org/10.7759/..

6

Maternal Prenatal Exposures in Pregnancy and Autism Spectru..:

, In: Advances in Neurobiology; Personalized Food Intervention and Therapy for Autism Spectrum Disorder Management,

Bastaki, Kholoud N. ; Alwan, Sura ; Zahir, Farah R. - p. 143-162 , 2020

Link: https://doi.org/10.1007/..

7

De novo pathogenic DNM1L variant in a patient diagnosed wit..:

Tarailo‐Graovac, Maja ; Zahir, Farah R. ; Zivkovic, Irena...
Molecular Genetics & Genomic Medicine. 7 (2019) 10 - p. , 2019

Link: https://doi.org/10.1002/..

8

A distinct neurodevelopmental syndrome with intellectual di..:

Yasin, Heba ; Gibson, William T. ; Langlois, Sylvie...
Journal of Human Genetics. 64 (2019) 4 - p. 271-280 , 2019

Link: https://doi.org/10.1038/..

9

Comprehensive whole genome sequence analyses yields novel g..:

Zahir, Farah R. ; Mwenifumbo, Jill C. ; Chun, Hye-Jung E....
BMC Genomics. 18 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

10

Intragenic CNVs for epigenetic regulatory genes in intellec..:

Zahir, Farah R. ; Tucker, Tracy ; Mayo, Sonia...
American Journal of Medical Genetics Part A. 170 (2016) 11 - p. 2916-2926 , 2016

Link: https://doi.org/10.1002/..

11

Use of Affymetrix Arrays in the Diagnosis of Gene Copy‐Numb..:

Zahir, Farah R. ; Marra, Marco A.
Current Protocols in Human Genetics. 85 (2015) 1 - p. , 2015

Link: https://doi.org/10.1002/..

12

Mutations in NGLY1 cause an inherited disorder of the endop..:

Enns, Gregory M. ; Shashi, Vandana ; Bainbridge, Matthew...
Genetics in Medicine. 16 (2014) 10 - p. 751-758 , 2014

Link: https://doi.org/10.1038/..

13

Book Review Genomics and Health in the Developing World. Ed..:

Zahir, Farah R.
American Journal of Medical Genetics Part A. 161 (2013) 5 - p. 1203-1206 , 2013

Link: https://doi.org/10.1002/..

14

Life‐history chronicle for a patient with the recently desc..:

Tsang, Erica ; Rupps, Rosemarie ; McGillivray, Barbara...
American Journal of Medical Genetics Part A. 158A (2012) 10 - p. 2606-2609 , 2012

Link: https://doi.org/10.1002/..

15

Detection of pathogenic copy number variants in children wi..:

Friedman, JM ; Adam, Shelin ; Arbour, Laura...
BMC Genomics. 10 (2009) 1 - p. 526 , 2009

Link: https://doi.org/10.1186/..