Author
Robert H. Yolken
Johns Hopkins UniversityORCID 0000-0001-9902-1554Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2021-2026 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 45 mutual co-author linksMutual co-authors in cluster
5 papers
Recent·Most cited
- Genetic & Genomic MedicinemedRxivPreprintDOI 10.64898/2026.09.30.26364416
- Genetic & Genomic MedicinemedRxivPreprint
Genetic survey of biomarkers across pregnancy identifies pregnancy-specialized immune regulation
Merve Çakır, Michela Traglia, Stacey Alexeeff…·Lauren A. Weiss
The paper conducts a genetic analysis of immune biomarkers across pregnancy timepoints, identifying heritable and genome-wide significant associations and highlighting timepoint-specific and pregnancy-unique findings.
DOI 10.64898/2025.12.31.25343052 - Developmental BiologybioRxivPreprint
DISC1-PML protein interaction for congenital CMV infection-induced cortical neural progenitor deficit: perturbance of host signaling via viral IE1
Atsushi Saito, Stephanie K. Tankou, Kazuhiro Ishii…·Akira Sawa
This study identifies the role of CMV viral protein IE1 in disrupting host DISC1-PML interaction, leading to neural progenitor deficits in congenital CMV infection.
DOI 10.1101/2025.09.03.674025 - Molecular BiologyAutism ResearchPeer-reviewed
Maternal antibodies to gliadin and autism spectrum disorders in offspring - A population-based case-control study in Sweden
Renee M. Gardner, Ida Samuelsson, Emily G. Severance…·Håkan Karlsson
This study examines if high maternal levels of anti-gliadin antibodies during pregnancy and birth are linked to reduced odds of autism spectrum disorder with intellectual disability in offspring.
3 citations - Genetic & Genomic MedicinemedRxivPreprint
Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia
Duncan S. Palmer, Daniel P. Howrigan, Sinéad B. Chapman…·Benjamin M. Neale
The paper reports exome sequencing findings in bipolar disorder, identifying AKAP11 as a shared risk gene with schizophrenia through ultra-rare protein-truncating variants.
5 citations