Neveen A Soliman

10PUBLICATIONS
37CO-AUTHORS
Gene mappingTe whāomoomo i te tuku ihotanga Māori (conservation of Māori heritage)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Medical devices
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Publications (10)

|May 22, 2025
Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndrome.

Neveen A Soliman, Mohamed A Elmonem, Ahmed F El-Sayed

|Apr 17, 2025
Remembering Professor Bahia H. Moustafa (1948-2024).

Neveen A Soliman, Ihab Sakr Shaheen

|Oct 18, 2024
Epigenomic and phenotypic characterization of DEGCAGS syndrome.

Karim Karimi, Denisa Weis, Ingvild Aukrust

|Apr 29, 2024
The Egypt Genome Project.

Mohamed A Elmonem, Neveen A Soliman, Ahmed Moustafa

|May 20, 2022
Primary hyperoxaluria type 1 in developing countries: novel challenges in a new therapeutic era.

Neveen A Soliman, Sameh Mabrouk

|Apr 12, 2022
Newborn Screening: Review of its Impact for Cystinosis.

Katharina Hohenfellner, Ewa Elenberg, Gema Ariceta

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Frequent Collaborators

2 joint publications

Khaled Amer

2 joint publications

Mohamed A Elmonem

2 joint publications

Friedhelm Hildebrandt

1 joint publications

Sofia Douzgou Houge