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Scientific Reports|March 13, 2019
Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopiaSangeetha Vishweswaraiah, Joanna Swierkowska, Uppala Ratnamala, et al.
Investigative Ophthalmology & Visual Science|November 18, 2008
Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32Marzena Gajecka, Uppala Radhakrishna, Daniel Winters, et al.
International Journal of Molecular Sciences|July 14, 2023
Gender Influences Gut Microbiota among Patients with Irritable Bowel SyndromePaulina Pecyna, Marcin Gabryel, Dorota Mankowska-Wierzbicka, et al.
European Journal of Human Genetics : EJHG|November 3, 2011
Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locusMarta Czugala, Justyna A Karolak, Dorota M Nowak, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|July 4, 2025
Blautia spp. in the gut microbiome: Relation to dietary choices and to the nutritional status of patients with irritable bowel syndromePaulina Pecyna, Aleksandra Bykowska-Derda, Marcin Gabryel, et al.
Investigative Ophthalmology & Visual Science|March 11, 2026
Common and Distinct Features in Serum Proteomic Profiles in Keratoconus, Post-Laser Vision Correction Ectasia, and Pellucid Marginal DegenerationKatarzyna Jaskiewicz-Rajewicz, Alicja Wysocka, Eliza Matuszewska-Mach, et al.
Genes|March 29, 2023
Prenatal Detection of a <i>FOXF1</i> Deletion in a Fetus with ACDMPV and HydronephrosisKatarzyna Bzdęga, Anna Kutkowska-Kaźmierczak, Gail H Deutsch, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closureMarzena Gajecka, Wei Yu, Blake C Ballif, et al.
American Journal of Medical Genetics. Part A|July 12, 2011
Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypesJill A Rosenfeld, Joanne Milisa Drautz, Carol L Clericuzio, et al.
European Journal of Human Genetics : EJHG|June 23, 2011
Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic functionAlex R Paciorkowski, Liu Lin Thio, Jill A Rosenfeld, et al.
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