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Connor P Hayes

5PUBLICATIONS

18CO-AUTHORS

Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesNeurogeneticsPredictive and prognostic markersGene expression (incl. microarray and other genome-wide approaches)

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Publications (5)

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|Feb 26, 2025

Novel <i>TBR1</i> c.1303C>T Variant Led to Diagnosis of Intellectual Developmental Disorder with Autism and Speech Delay: Application of Comprehensive Family-Based Whole-Genome Analysis.

Mario Ćuk, Busra Unal, Matea Bagarić

|Oct 26, 2024

Novel Variant in <i>ANO5</i> Muscular Dystrophy: Identification by Whole Genome Sequencing and Quad Analysis.

Mario Ćuk, Busra Unal, Luka Lovrenčić

|Jul 12, 2024

Novel de Novo Nonsense Variants in AGO3 and KHSRP: Insights into Global Developmental Delay and Autism Spectrum Disorders through Whole Genome Analysis.

Mario Ćuk, Luka Lovrenčić, Busra Unal

|Apr 19, 2024

Germline and Somatic Fumarate Hydratase Testing in Atypical Uterine Leiomyomata.

Lindsay M Kipnis, Katelyn M Breen, Diane R Koeller

|Feb 03, 2024

Genomic disparity impacts variant classification of cancer susceptibility genes in Turkish breast cancer patients.

Nihat B Agaoglu, Busra Unal, Connor P Hayes

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Frequent Collaborators

4 joint publications

Arezou A Ghazani

2 joint publications

Goran Krakar

2 joint publications

Busra Unal

2 joint publications

Mario Ćuk

2 joint publications

Luka Lovrenčić

1 joint publications

Nihat B Agaoglu

1 joint publications

Lindsay M Kipnis

1 joint publications

Diane R Koeller

1 joint publications

Alison Schwartz Levine

1 joint publications

Hyeji Jun

Frequent Collaborators

4 joint publications

Arezou A Ghazani

2 joint publications

Goran Krakar

2 joint publications

Busra Unal

2 joint publications

Mario Ćuk

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