Hans-Hilger Ropers

ORCID

Publication Activity (10 Years)

Years Active: 2018-2020
Publications (10 Years): 3

Top Venues

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Maryam Beheshtian, Tara Akhtarkhavari, Sepideh Mehvari, Marzieh Mohseni, Zohreh Fattahi, Seyedeh Sedigheh Abedini, Sanaz Arzhangi, Mahsa Fadaee, Payman Jamali, Reza Najafipour, Vera M Kalscheuer, Hao Hu, Hans-Hilger Ropers, Hossein Najmabadi, Kimia Kahrizi
Comprehensive genotype-phenotype correlation in AP-4 deficiency syndrome; Adding data from a large cohort of Iranian patients. Clinical genetics 99 (1) (2020)
Maryam Beheshtian, Zohreh Fattahi, Mahsa Fadaee, Raheleh Vazehan, Payman Jamali, Elham Parsimehr, Mahboubeh Kamgar, Mehrshid Faraji Zonooz, Shokouh Sadat Mahdavi, Zahra Kalhor, Sanaz Arzhangi, Seyedeh Sedigheh Abedini, Farahnaz Sabbagh Kermani, Faezeh Mojahedi, Vera M Kalscheuer, Hans-Hilger Ropers, Ariana Kariminejad, Hossein Najmabadi, Kimia Kahrizi
Identification of disease-causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families. Clinical genetics 95 (6) (2019)
Kimia Kahrizi, Hao Hu, Masoumeh Hosseini, Vera M Kalscheuer, Zohreh Fattahi, Maryam Beheshtian, Vanessa Suckow, Marzieh Mohseni, Bettina Lipkowitz, Sepideh Mehvari, Zohreh Mehrjoo, Tara Akhtarkhavari, Zhila Ghaderi, Maryam Rahimi, Sanaz Arzhangi, Payman Jamali, Milad Falahat Chian, Pooneh Nikuei, Farahnaz Sabbagh Kermani, Farnaz Sadeghinia, Roshanak Jazayeri, S Hassan Tonekaboni, Atefeh Khoshaeen, Haleh Habibi, Fatemeh Pourfatemi, Faezeh Mojahedi, Mohammad-Reza Khodaie-Ardakani, Reza Najafipour, Thomas F Wienker, Hossein Najmabadi, Hans-Hilger Ropers
Effect of inbreeding on intellectual disability revisited by trio sequencing. Clinical genetics 95 (1) (2018)

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Publication Activity (10 Years)

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Top Venues

Hans-Hilger Ropers