Multidisciplinary management of a patient with van der Woude syndrome: A case report

door Tehranchi, Azita, Behnia, Hossein, Nadjmi, Nasser, Yassaee, Vahid Reza, Ravesh, Zeinab, Mina, Morteza
Gepubliceerd in Int J Surg Case Rep (2016)

Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

door Ravesh, Zeinab, Dianatpour, Mahdi, Fardaei, Majid, Taghdiri, Maryam, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Miryounesi, Mohammad
Gepubliceerd in Mol Vis (2018)

Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies

door Salmaninejad, Arash, Bedoni, Nicola, Ravesh, Zeinab, Quinodoz, Mathieu, Shoeibi, Nasser, Mojarrad, Majid, Pasdar, Alireza, Rivolta, Carlo
Gepubliceerd in Sci Rep (2020)

Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populations

door Eaaswarkhanth, Muthukrishnan, Haque, Ikramul, Ravesh, Zeinab, Romero, Irene Gallego, Meganathan, Poorlin Ramakodi, Dubey, Bhawna, Khan, Faizan Ahmed, Chaubey, Gyaneshwer, Kivisild, Toomas, Tyler-Smith, Chris, Singh, Lalji, Thangaraj, Kumarasamy
Gepubliceerd in 2010

Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin

door Ravesh, Zeinab, El Asrag, Mohammed E., Weisschuh, Nicole, McKibbin, Martin, Reuter, Peggy, Watson, Christopher M., Baumann, Britta, Poulter, James A., Sajid, Sundus, Panagiotou, Evangelia S., O’Sullivan, James, Abdelhamed, Zakia, Bonin, Michael, Soltanifar, Mehdi, Black, Graeme C.M., Din, Muhammad Amin-ud, Toomes, Carmel, Ansar, Muhammad, Inglehearn, Chris F., Wissinger, Bernd, Ali, Manir
Gepubliceerd in Mol Vis (2015)