| Periodontal Manifestation of Type Ib Glycogen Storage Disease: A Rare Case Report | Dababneh, R., Shawabkeh, A., Gharaibeh, S., ...Amayreh, W., Bissada, N.F. | Clinical advances in periodontics | ---- | ---- | 2020 |
| Novel mutations in the SMPD1 gene in Jordanian children with Acid sphingomyelinase deficiency (Niemann-Pick types A and B) | AL-Eitan, L., Alqa'qa', K., Amayreh, W., ...Haddad, Y., Haddad, H. | Gene | 15;747:144683. | ---- | July 2020 |
| Identification and characterization of BTD gene mutations in jordanian children with biotinidase deficiency | Al‐eitan, L.N., Alqa’qa’, K., Amayreh, W., ...Jaradat, Z., Haddad, H. | Journal of Personalized Medicine | ---- | ---- | 2020 Jan |
| Molecular genetics of phenylketonuria and tetrahydrobiopterin deficiency in Jordan | Carducci, C., Amayreh, W., Ababneh, H., ...Hoffmann, G.F., Blau, N. | JIMD Reports | ---- | ---- | 2020 May |
| Molecular analysis of maple syrup urine disease in Jordanian families | Jaradat, S.A., Al-Qa'qa', K., Amayreh, W., ...Deebajah, H., Al Rababah, B. | Meta Gene | ---- | Elsevier | Dec 2016 |
| Molecular analysis of LPIN1 in Jordanian patients with rhabdomyolysis | Jaradat, S.A., Amayreh, W., Al-Qa'qa', K., Krayyem, J. | Meta Gene | 7 | Elsevier | 2015 Dec |
| Treatment of arginase deficiency revisited: Guanidinoacetate as a therapeutic target and biomarker for therapeutic monitoring | Amayreh, W., Meyer, U., Das, A.M. | Dev Med Child Neurol | ---- | Wiley | 2014 Oct |