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Author/Creator Faghihi, Mohammad A.

1. Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short stature. Issue 1 (30th November 2020)

Authors:
Ain, Noor U.; Muhammad, Niaz; Dianatpour, Mehdi; Baroncelli, Marta; Iqbal, Muddassar; Fard, Mohammad A. F.; Bukhari, Ihtisham; Ahmed, Sufian; Hajipour, Massoumeh; Tabatabaie, Zahra; Foroutan, Hamidreza; Nilsson, Ola; Faghihi, Mohammad A.; Makitie, Outi; Naz, Sadaf
Journal:
Human mutation
Issue:
Volume 42:Issue 1(2021)
Page Start:
89
Record Type:
Journal Article
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2. Expanding the molecular and clinical phenotypes of FUT8‐CDG. Issue 4 (23rd February 2020)

Authors:
Ng, Bobby G.; Dastsooz, Hassan; Silawi, Mohammad; Habibzadeh, Parham; Jahan, Shima B.; Fard, Mohammad A. F.; Halliday, Benjamin J.; Raymond, Kimiyo; Ruzhnikov, Maura R. Z.; Tabatabaei, Zahra; Taghipour‐Sheshdeh, Afsaneh; Brimble, Elise; Robertson, Stephen P.; Faghihi, Mohammad A.; Freeze, Hudson H.
Journal:
Journal of inherited metabolic disease
Issue:
Volume 43:Issue 4(2020)
Page Start:
871
Record Type:
Journal Article
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3. Ketamine up-regulates a cluster of intronic miRNAs within the serotonin receptor 2C gene by inhibiting glycogen synthase kinase-3. (18th August 2017)

Authors:
Grieco, Steven F.; Velmeshev, Dmitry; Magistri, Marco; Eldar-Finkelman, Hagit; Faghihi, Mohammad A.; Jope, Richard S.; Beurel, Eleonore
Journal:
World journal of biological psychiatry
Issue:
Volume 18:Number 6(2017)
Page Start:
445
Record Type:
Journal Article
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