Author

Nitza Newman

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Open access Oct 2026

Identification of a novel candidate locus at 21q22.3 for isolated intestinal Malrotation

Abstract Intestinal malrotation (IM) is a relatively common congenital anomaly of the gastrointestinal tract resulting from abnormal rotation during embryonic development. While some cases of IM are part of syndromic manifestations, most are isolated, with their genetic basis remaining largely unknown. We present a fam...

Nadav Agam, Nitza Newman, V. Dolgin et al. · Human Molecular Genetics · 0 citations

Open access Oct 2026

Functional characterization of a non-coding RUNX1T1 variant in a kindred with esophageal atresia

Abstract Introduction Esophageal atresia (EA) is a congenital foregut malformation with substantial genetic heterogeneity. While coding variants explain some syndromic cases, the molecular basis of non-syndromic EA remains largely unknown. We investigated an Israeli-Bedouin kindred with a high incidence of non-syndromi...

Nadav Agam, Sarit Aharoni, B. Yerushalmi et al. · Organogenesis · 0 citations