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Author/Creator Ansar, Muhammad

1. A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair. Issue 10 (9th July 2015)

Authors:
Ansar, Muhammad; Raza, Syed Irfan; Lee, Kwanghyuk; Irfanullah, ; Shahi, Shamim; Acharya, Anushree; Dai, Hang; Smith, Joshua D; Shendure, Jay; Bamshad, Michael J; Nickerson, Deborah A; Santos-Cortez, Regie Lyn P; Ahmad, Wasim; Leal, Suzanne M
Other Names:
contributor.
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 10(2015)
Page Start:
676
Record Type:
Journal Article
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3. A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations. Issue 9 (25th July 2019)

Authors:
Parveen, Asia; Mirza, Muhammad U.; Vanmeert, Michiel; Akhtar, Javed; Bashir, Hina; Khan, Saadullah; Shehzad, Saqib; Froeyen, Matheus; Ahmed, Wasim; Ansar, Muhammad; Wasif, Naveed
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 9(2019)
Page Start:
n/a
Record Type:
Journal Article
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5. Biallelic missense variants in ZBTB11 can cause intellectual disability in humans. (8th June 2018)

Authors:
Fattahi, Zohreh; Sheikh, Taimoor I; Musante, Luciana; Rasheed, Memoona; Taskiran, Ibrahim Ihsan; Harripaul, Ricardo; Hu, Hao; Kazeminasab, Somayeh; Alam, Muhammad Rizwan; Hosseini, Masoumeh; Larti, Farzaneh; Ghaderi, Zhila; Celik, Arzu; Ayub, Muhammad; Ansar, Muhammad; Haddadi, Mohammad; Wienker,...
Journal:
Human molecular genetics
Issue:
Volume 27:Number 18(2018:Sep. 15)
Page Start:
3177
Record Type:
Journal Article
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6. Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature. (4th March 2020)

Authors:
Ansar, Muhammad; Ebstein, Frédéric; Özkoç, Hayriye; Paracha, Sohail A; Iwaszkiewicz, Justyna; Gesemann, Matthias; Zoete, Vincent; Ranza, Emmanuelle; Santoni, Federico A; Sarwar, Muhammad T; Ahmed, Jawad; Krüger, Elke; Bachmann-Gagescu, Ruxandra; Antonarakis, Stylianos E
Journal:
Human molecular genetics
Issue:
Volume 29:Number 7(2020)
Page Start:
1132
Record Type:
Journal Article
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7. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021)

Authors:
Poulter, James A.; Gravett, Molly S. C.; Taylor, Rachel L.; Fujinami, Kaoru; De Zaeytijd, Julie; Bellingham, James; Rehman, Atta Ur; Hayashi, Takaaki; Kondo, Mineo; Rehman, Abdur; Ansar, Muhammad; Donnelly, Dan; Toomes, Carmel; Ali, Manir; De Baere, Elfride; Leroy, Bart P.; Davies, Nigel P.; Hend...
Journal:
Human mutation
Issue:
Volume 42:Issue 2(2021)
Page Start:
ii
Record Type:
Journal Article
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8. Depth Distribution of Soil Organic Carbon Fractions in Relation to Tillage and Cropping Sequences in Some Dry Lands of Punjab, Pakistan. (17th March 2015)

Authors:
Hassan, Asma; Ijaz, Shahzada Sohail; Lal, Rattan; Ali, Safdar; Hussain, Qaiser; Ansar, Muhammad; Khattak, Romaan Hayat; Baloch, Muhammad Sharif
Journal:
Land degradation & development
Issue:
Volume 27:Number 4(2016)
Page Start:
1175
Record Type:
Journal Article
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9. Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2. Issue 1 (9th March 2021)

Authors:
Antonarakis, Stylianos E; Holoubek, Aleš; Rapti, Melivoia; Rademaker, Jesse; Meylan, Jenny; Iwaszkiewicz, Justyna; Zoete, Vincent; Wilson, Callum; Taylor, Juliet; Ansar, Muhammad; Borel, Christelle; Menzel, Olivier; Kuželová, Kateřina; Santoni, Federico A
Journal:
Human molecular genetics
Issue:
Volume 31:Issue 1(2022)
Page Start:
1
Record Type:
Journal Article
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10. Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree. Issue 1 (December 2016)

Authors:
Makrythanasis, Periklis; Guipponi, Michel; Santoni, Federico; Zaki, Maha; Issa, Mahmoud; Ansar, Muhammad; Hamamy, Hanan; Antonarakis, Stylianos
Journal:
Human genomics
Issue:
Volume 10:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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