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Author Details
Full Name
Leila Jamal
Affiliation
Center for Cancer Research, National Cancer Institute
ORCID
Career Start Year
2012
Papers
26
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37641538
Research participants' perspectives about the return of uninformative genomic test results in a clinical research setting.
J Genet Couns
2024
35263009
National Society of Genetic Counselors' Board of Directors response to Myers et al. 'A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination'.
J Genet Couns
2022
35476126
The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome.
Blood Adv
2022
35753512
Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations.
J Allergy Clin Immunol
2022
36715254
Reason-Based Abortion Bans, Disability Rights, and the Future of Prenatal Genetic Testing.
Am J Law Med
2022
35980380
Genomic tools for health: Secondary findings as findings to be shared.
Genet Med
2022
33320394
Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict.
J Genet Couns
2021
33620774
The Ethics of Repurposing Previously Collected Research Biospecimens in an Infectious Disease Pandemic.
Ethics Hum Res
2021
32557217
Re-examining the Ethics of Genetic Counselling in the Genomic Era.
J Bioeth Inq
2020
31856388
An ethical framework for genetic counseling in the genomic era.
J Genet Couns
2020
30680845
Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
J Genet Couns
2019
30951675
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Am J Hum Genet
2019
30011896
Synthetic Cannabinoid use in a Case Series of Patients with Psychosis Presenting to Acute Psychiatric Settings: Clinical Presentation and Management Issues.
Brain Sci
2018
28949844
When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing.
AJOB Empir Bioeth
2017
28218387
Defining personal utility in genomics: A Delphi study.
Clin Genet
2017
26080898
Are physicians prepared for whole genome sequencing? a qualitative analysis.
Clin Genet
2016
27019659
Patients' perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project.
Per Med
2016
27047759
An old problem in a new age: Revisiting the clinical dilemma of misattributed paternity.
Appl Transl Genom
2016
25045831
Living laboratory: whole-genome sequencing as a learning healthcare enterprise.
Clin Genet
2015
26174511
Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome.
Am J Med Genet A
2015
23576233
'Out of hours' adult CT head interpretation by senior emergency department staff following an intensive teaching session: a prospective blinded pilot study of 405 patients.
Emerg Med J
2014
25131622
Clinical whole exome sequencing in child neurology practice.
Ann Neurol
2014
24705284
Revisiting respect for persons in genomic research.
Genes (Basel)
2014
24281371
Research participants' attitudes towards the confidentiality of genomic sequence information.
Eur J Hum Genet
2014
24126608
Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly.
JAMA Neurol
2013
22578482
Association between polycystic ovarian syndrome, overweight, and metabolic syndrome in adolescents.
J Pediatr Adolesc Gynecol
2012
1 - 26 of 26
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Harvard Medical School
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