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Leila Jamal
Leila Jamal
在 nih.gov 的电子邮件经过验证
标题
引用次数
引用次数
年份
Clinical whole exome sequencing in child neurology practice
S Srivastava, JS Cohen, H Vernon, K Barañano, R McClellan, L Jamal, ...
Annals of neurology 76 (4), 473-483, 2014
3062014
Are physicians prepared for whole genome sequencing? A qualitative analysis
KD Christensen, JL Vassy, L Jamal, LS Lehmann, MJ Slashinski, ...
Clinical genetics 89 (2), 228-234, 2016
1342016
The responsibility to recontact research participants after reinterpretation of genetic and genomic research results
Y Bombard, KB Brothers, S Fitzgerald-Butt, G Nanibaa’A, L Jamal, ...
The American Journal of Human Genetics 104 (4), 578-595, 2019
1202019
Defining personal utility in genomics: a Delphi study
JN Kohler, E Turbitt, KL Lewis, BS Wilfond, L Jamal, HL Peay, ...
Clinical genetics 92 (3), 290-297, 2017
822017
Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly
C Gonzaga-Jauregui, T Lotze, L Jamal, S Penney, IM Campbell, ...
JAMA neurology 70 (12), 1491-1498, 2013
702013
Research participants’ attitudes towards the confidentiality of genomic sequence information
L Jamal, JC Sapp, K Lewis, T Yanes, FM Facio, LG Biesecker, ...
European Journal of Human Genetics 22 (8), 964-968, 2014
682014
An ethical framework for genetic counseling in the genomic era
L Jamal, W Schupmann, BE Berkman
Journal of Genetic Counseling 29 (5), 718-727, 2020
572020
An old problem in a new age: Revisiting the clinical dilemma of misattributed paternity
L Hercher, L Jamal
Applied & Translational Genomics 8, 36-39, 2016
452016
Patients’ perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project
PJ Lupo, JO Robinson, PM Diamond, L Jamal, HE Danysh, ...
Personalized medicine 13 (1), 13-20, 2016
452016
When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing
L Jamal, JO Robinson, KD Christensen, J Blumenthal-Barby, ...
AJOB empirical bioethics 8 (2), 82-88, 2017
432017
Precision population medicine in primary care: the Sanford Chip experience
KD Christensen, M Bell, CLB Zawatsky, LN Galbraith, RC Green, ...
Frontiers in Genetics 12, 626845, 2021
352021
Improved provider preparedness through an 8-part genetics and genomic education program
C Hajek, AM Hutchinson, LN Galbraith, RC Green, MF Murray, N Petry, ...
Genetics in Medicine 24 (1), 214-224, 2022
302022
Living laboratory: whole‐genome sequencing as a learning healthcare enterprise
M Angrist, L Jamal
Clinical Genetics 87 (4), 311-318, 2015
272015
Revisiting respect for persons in genomic research
DJH Mathews, L Jamal
Genes 5 (1), 1-12, 2014
272014
Re-examining the ethics of genetic counselling in the genomic era
W Schupmann, L Jamal, BE Berkman
Journal of Bioethical Inquiry 17 (3), 325-335, 2020
202020
Clinical exome sequencing of 1000 families with complex immune phenotypes: toward comprehensive genomic evaluations
MN Similuk, J Yan, R Ghosh, AJ Oler, LM Franco, MR Setzer, M Kamen, ...
Journal of Allergy and Clinical Immunology 150 (4), 947-954, 2022
192022
Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions
X Li, R Nusbaum, C Smith‐Hicks, L Jamal, S Dixon, S Mahida
Journal of Genetic Counseling 28 (2), 304-312, 2019
182019
New modes of engagement for big data research
DE Winickoff, L Jamal, NR Anderson
Journal of Responsible Innovation 3 (2), 169-177, 2016
172016
Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome
S Tunovic, KW Barañano, JA Barkovich, JB Strober, L Jamal, ...
American journal of medical genetics Part A 167 (11), 2767-2776, 2015
142015
Genomic tools for health: Secondary findings as findings to be shared
SA Miner, M Similuk, L Jamal, J Sapp, BE Berkman
Genetics in Medicine 24 (11), 2220-2227, 2022
72022
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