1.
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
by Chong, Jessica X
American journal of human genetics, 2015-08-06, Vol.97 (2), p.199-215
2.
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants
by Kearney, Hutton M.
Genetics in medicine, 2011-07, Vol.13 (7), p.680-685
3.
Finding the missing heritability of complex diseases
by Haines, Jonathan L
Nature (London), 2009-10-08, Vol.461 (7265), p.747-753
4.
Structural Variation of Chromosomes in Autism Spectrum Disorder
by Marshall, Christian R
American journal of human genetics, 2008, Vol.82 (2), p.477-488
5.
Managing incidental findings and research results in genomic research involving biobanks and archived data sets
by Wolf, Susan M
Genetics in medicine, 2012-04, Vol.14 (4), p.361-384
6.
Estimating Local Ancestry in Admixed Populations
by Sankararaman, Sriram
American journal of human genetics, 2008, Vol.82 (2), p.290-303
7.
ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing
by Hickey, Scott E
Genetics in medicine, 2013-02, Vol.15 (2), p.153-156
8.
The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists
by Boycott, Kym
Journal of medical genetics, 2015-07, Vol.52 (7), p.431-437
9.
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila
by Zweier, Christiane
American journal of human genetics, 2009-11-13, Vol.85 (5), p.655-666
10.
Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study
by Bollinger, Juli Murphy
Genetics in medicine, 2012-04, Vol.14 (4), p.451-457
11.
An agenda for personalized medicine
by Ng, Pauline C
Nature (London), 2009-10-08, Vol.461 (7265), p.724-726
12.
The promise of whole-exome sequencing in medical genetics
by Rabbani, Bahareh
Journal of human genetics, 2014-01, Vol.59 (1), p.5-15
13.
Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project
by Biesecker, Leslie G
Genetics in medicine, 2012-04, Vol.14 (4), p.393-398
14.
Epistasis and Its Implications for Personal Genetics
by Moore, Jason H
American journal of human genetics, 2009, Vol.85 (3), p.309-320
15.
Recent advances in the genetics of sarcoidosis
by Spagnolo, Paolo
Journal of Medical Genetics, 2013-05, Vol.50 (5), p.290-414
16.
Genotype-Imputation Accuracy across Worldwide Human Populations
by Huang, Lucy
American journal of human genetics, 2009-02-13, Vol.84 (2), p.235-250
17.
Translational Genomics in Low- and Middle-Income Countries: Opportunities and Challenges
by Tekola-Ayele, Fasil
Community genetics, 2015-01-01, Vol.18 (4), p.242-247
18.
NEK1 Mutations Cause Short-Rib Polydactyly Syndrome Type Majewski
by Thiel, Christian
American journal of human genetics, 2011-01-07, Vol.88 (1), p.106-114
19.
The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues
by Hogarth, Stuart
Annual review of genomics and human genetics, 2008, Vol.9 (1), p.161-182
20.
A Geographically Explicit Genetic Model of Worldwide Human-Settlement History
by Liu, Hua
American journal of human genetics, 2006, Vol.79 (2), p.230-237
