Clara Lajonchere

APLA Health — United States

Neuroscience · Life Sciences

32h-index9.7kcitations72works1.52yr avg
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Research Topics

Autism Spectrum Disorder Research(25), Genomics and Rare Diseases(15), Genomic variations and chromosomal abnormalities(14), Genetics and Neurodevelopmental Disorders(13), Ethics in Clinical Research(12)

Publications69 total

Advancing Precision Health Discovery in a Genetically Diverse Health System
2025· 1 citedOpen Access
Assessing perceived empathy based on genetic counselor gender using a randomized, hypothetical prenatal genetic counseling scenario design
Journal of Genetic Counseling·2025Open Access
Abstract 3244: <i>cfTrack-methyl</i>: A personalized approach using cfDNA methylomes for ultra-sensitive MRD detection
Cancer Research·2025
Cross-sectional Analysis of Exome Sequencing Diagnosis in Patients with Neurologic Phenotypes Facing Barriers to Clinical Testing (P1-1.009)
Neurology·2025
Exploring perceptions of genetic counseling student‐run free clinics as an innovative service delivery model to increase access to genetic counseling services
Journal of Genetic Counseling·2024· 1 citedOpen Access
Author Correction: Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer
Nature Communications·2024· 1 citedOpen Access
Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing
Neurology Genetics·2024· 7 citedOpen Access
Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer’s Disease
2024· 2 citedOpen Access
The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank
Cell Genomics·2023· 32 citedOpen Access
Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Genome Medicine·2022· 4 citedOpen Access
Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer
Nature Communications·2022· 107 citedOpen Access
Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Genome Medicine·2022· 47 citedOpen Access
The UCLA ATLAS Community Health Initiative: promoting precision health research in a diverse biobank
2022· 9 citedOpen Access
Additional file 2 of Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Figshare·2022Open Access
Additional file 6 of Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Figshare·2022Open Access
Additional file 4 of Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Figshare·2022Open Access
Additional file 3 of Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Figshare·2022Open Access
Global Biobank Meta-analysis Initiative: powering genetic discovery across human diseases
2021· 60 citedOpen Access
Correction: Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
JMIR Formative Research·2021· 3 citedOpen Access
Correction: Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study (Preprint)
2021Open Access
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Frequent Co-authors

Daniel H. Geschwind(14), Géraldine Dawson(7), Nancy J. Minshew(7), Clara E. Magyar(7), Sarah Dry(7), Annette Estes(6), Joseph Glessner(6), Vlad Kustanovich(6), Linda Lotspeich(6), Deborah L. Levy(6), Bogdan Paşaniuc(6), Brett S. Abrahams(5), Jennifer Howe(5), Christian R. Marshall(5), William M. McMahon(5), Joseph Piven(5), Rita M. Cantor(5), Arjun Bhattacharya(5), Yi Ding(5), Ruth Johnson(5)