Erica E Davis

25PUBLICATIONS

204CO-AUTHORS

Medical biotechnology diagnostics (incl. biosensors)Cell and nuclear divisionGene mappingEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)

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Publications (25)

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|May 23, 2026

Streamlining Diagnosis of Bardet-Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria.

|Oct 17, 2025

CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies.

Kamal Khan, Erika Tavares, Katherine Bishara

|Aug 27, 2025

Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz-Jeghers Syndrome.

Tahir N Khan, Chunyu Liu, Kai Lee Yap

|Feb 17, 2025

RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.

Avinash V Dharmadhikari, Maria Alba Abad, Sheraz Khan

|Sep 10, 2024

Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors.

Jana Willim, Daniel Woike, Daniel Greene

|Jul 15, 2024

Pathogenic variants in <i>TMEM184B</i> cause a neurodevelopmental syndrome associated with alteration of metabolic signaling.

Kimberly A Chapman, Farid Ullah, Zachary A Yahiku

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Frequent Collaborators

Nicholas Katsanis

Farid Ullah

Seth I Berger

Martha Rc Bhattacharya

Kelvin W Pond

Suman Sirimulla

Tahir N Khan

Kimberly A Chapman

Humayoon Shafique Satti

2 joint publications

Antonio Vitobello

Frequent Collaborators

Nicholas Katsanis

Farid Ullah

Seth I Berger

Martha Rc Bhattacharya