Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2012 | 1 |
2013 | 1 |
2014 | 3 |
2015 | 3 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Communicating genetic risk information for common disorders in the era of genomic medicine.
Annu Rev Genomics Hum Genet. 2013;14:491-513. doi: 10.1146/annurev-genom-092010-110722.
Annu Rev Genomics Hum Genet. 2013.
PMID: 24003856
Free PMC article.
Review.
Factors affecting recall of different types of personal genetic information about Alzheimer's disease risk: the REVEAL study.
Besser AG, Sanderson SC, Roberts JS, Chen CA, Christensen KD, Lautenbach DM, Cupples LA, Green RC.
Besser AG, et al. Among authors: lautenbach dm.
Public Health Genomics. 2015;18(2):78-86. doi: 10.1159/000368888. Epub 2015 Jan 24.
Public Health Genomics. 2015.
PMID: 25634646
Free PMC article.
Clinical Trial.
Item in Clipboard
The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Vassy JL, Lautenbach DM, McLaughlin HM, Kong SW, Christensen KD, Krier J, Kohane IS, Feuerman LZ, Blumenthal-Barby J, Roberts JS, Lehmann LS, Ho CY, Ubel PA, MacRae CA, Seidman CE, Murray MF, McGuire AL, Rehm HL, Green RC; MedSeq Project.
Vassy JL, et al. Among authors: lautenbach dm.
Trials. 2014 Mar 20;15:85. doi: 10.1186/1745-6215-15-85.
Trials. 2014.
PMID: 24645908
Free PMC article.
Clinical Trial.
Item in Clipboard
Summarizing polygenic risks for complex diseases in a clinical whole-genome report.
Kong SW, Lee IH, Leshchiner I, Krier J, Kraft P, Rehm HL, Green RC, Kohane IS, MacRae CA; MedSeq Project.
Kong SW, et al.
Genet Med. 2015 Jul;17(7):536-44. doi: 10.1038/gim.2014.143. Epub 2014 Oct 23.
Genet Med. 2015.
PMID: 25341114
Free PMC article.
Item in Clipboard
A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
McLaughlin HM, Ceyhan-Birsoy O, Christensen KD, Kohane IS, Krier J, Lane WJ, Lautenbach D, Lebo MS, Machini K, MacRae CA, Azzariti DR, Murray MF, Seidman CE, Vassy JL, Green RC, Rehm HL; MedSeq Project.
McLaughlin HM, et al.
BMC Med Genet. 2014 Dec 14;15:134. doi: 10.1186/s12881-014-0134-1.
BMC Med Genet. 2014.
PMID: 25714468
Free PMC article.
Item in Clipboard
'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project.
Vassy JL, Christensen KD, Slashinski MJ, Lautenbach DM, Raghavan S, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Lehmann LS, Murray MF, Green RC, McGuire AL.
Vassy JL, et al. Among authors: lautenbach dm.
Per Med. 2015;12(1):23-32. doi: 10.2217/pme.14.68.
Per Med. 2015.
PMID: 25642274
Free PMC article.
Item in Clipboard
Mothers' perspectives on their child's mental illness as compared to other complex disorders in their family: insights to inform genetic counseling practice.
Lautenbach DM, Hiraki S, Campion MW, Austin JC.
Lautenbach DM, et al.
J Genet Couns. 2012 Aug;21(4):564-72. doi: 10.1007/s10897-011-9420-7. Epub 2011 Nov 17.
J Genet Couns. 2012.
PMID: 22089936
Free PMC article.
Item in Clipboard
Cite
Cite