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Author/Creator Beheshtian, Maryam

1. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. Issue 12 (7th October 2015)

Authors:
Sloan-Heggen, Christina M; Babanejad, Mojgan; Beheshtian, Maryam; Simpson, Allen C; Booth, Kevin T; Ardalani, Fariba; Frees, Kathy L; Mohseni, Marzieh; Mozafari, Reza; Mehrjoo, Zohreh; Jamali, Leila; Vaziri, Saeideh; Akhtarkhavari, Tara; Bazazzadegan, Niloofar; Nikzat, Nooshin; Arzhangi, Sanaz; S...
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 12(2015)
Page Start:
823
Record Type:
Journal Article
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2. Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients. Issue 1 (14th September 2020)

Authors:
Beheshtian, Maryam; Akhtarkhavari, Tara; Mehvari, Sepideh; Mohseni, Marzieh; Fattahi, Zohreh; Abedini, Seyedeh Sedigheh; Arzhangi, Sanaz; Fadaee, Mahsa; Jamali, Payman; Najafipour, Reza; Kalscheuer, Vera M.; Hu, Hao; Ropers, Hans‐Hilger; Najmabadi, Hossein; Kahrizi, Kimia
Journal:
Clinical genetics
Issue:
Volume 99:Issue 1(2021)
Page Start:
187
Record Type:
Journal Article
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3. Effect of inbreeding on intellectual disability revisited by trio sequencing. Issue 1 (19th November 2018)

Authors:
Kahrizi, Kimia; Hu, Hao; Hosseini, Masoumeh; Kalscheuer, Vera M.; Fattahi, Zohreh; Beheshtian, Maryam; Suckow, Vanessa; Mohseni, Marzieh; Lipkowitz, Bettina; Mehvari, Sepideh; Mehrjoo, Zohreh; Akhtarkhavari, Tara; Ghaderi, Zhila; Rahimi, Maryam; Arzhangi, Sanaz; Jamali, Payman; Falahat Chian, Mil...
Journal:
Clinical genetics
Issue:
Volume 95:Issue 1(2019)
Page Start:
151
Record Type:
Journal Article
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4. Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran. Issue 1 (24th March 2021)

Authors:
Mohseni, Marzieh; Babanejad, Mojgan; Booth, Kevin T.; Jamali, Payman; Jalalvand, Khadijeh; Davarnia, Behzad; Ardalani, Fariba; Khoshaeen, Atefeh; Arzhangi, Sanaz; Ghodratpour, Fatemeh; Beheshtian, Maryam; Jahanshad, Faezeh; Otukesh, Hasan; Bahrami, Fatemeh; Seifati, Seyed Morteza; Bazazzadegan, N...
Journal:
Clinical genetics
Issue:
Volume 100:Issue 1(2021)
Page Start:
59
Record Type:
Journal Article
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5. Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families. Issue 6 (14th May 2019)

Authors:
Beheshtian, Maryam; Fattahi, Zohreh; Fadaee, Mahsa; Vazehan, Raheleh; Jamali, Payman; Parsimehr, Elham; Kamgar, Mahboubeh; Zonooz, Mehrshid Faraji; Mahdavi, Shokouh Sadat; Kalhor, Zahra; Arzhangi, Sanaz; Abedini, Seyedeh Sedigheh; Kermani, Farahnaz Sabbagh; Mojahedi, Faezeh; Kalscheuer, Vera M.; ...
Journal:
Clinical genetics
Issue:
Volume 95:Issue 6(2019)
Page Start:
718
Record Type:
Journal Article
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6. Iranome: A catalog of genomic variations in the Iranian population. Issue 11 (17th August 2019)

Authors:
Fattahi, Zohreh; Beheshtian, Maryam; Mohseni, Marzieh; Poustchi, Hossein; Sellars, Erin; Nezhadi, Sayyed Hossein; Amini, Amir; Arzhangi, Sanaz; Jalalvand, Khadijeh; Jamali, Peyman; Mohammadi, Zahra; Davarnia, Behzad; Nikuei, Pooneh; Oladnabi, Morteza; Mohammadzadeh, Akbar; Zohrehvand, Elham;...
Journal:
Human mutation
Issue:
Volume 40:Issue 11(2019)
Page Start:
1968
Record Type:
Journal Article
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7. Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients. Issue 4 (17th February 2022)

Authors:
Mosallaei, Meysam; Ehtesham, Naeim; Beheshtian, Maryam; Khoshbakht, Shahrouz; Davarnia, Behzad; Kahrizi, Kimia; Najmabadi, Hossein
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 10:Issue 4(2022)
Page Start:
n/a
Record Type:
Journal Article
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9. Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability. Issue 10 (26th July 2020)

Authors:
Mehvari, Sepideh; Larti, Farzaneh; Hu, Hao; Fattahi, Zohreh; Beheshtian, Maryam; Abedini, Seyedeh Sedigheh; Arzhangi, Sanaz; Ropers, Hans‐Hilger; Kalscheuer, Vera M.; Auld, Daniel; Kahrizi, Kimia; Riazalhosseini, Yasser; Najmabadi, Hossein
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 10(2020)
Page Start:
n/a
Record Type:
Journal Article
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