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Author/Creator Ansar, Muhammad

1. Inability of the most commonly used forensic genetic markers to distinguish between samples belonging to different ethnicities of Pakistan with diverse genetic background. (May 2016)

Authors:
Chishti, Hafsah Muhammad; Manica, Andrea; Ansar, Muhammad; Eriksson, Anders; Ajmal, Muhammad; Hameed, Abdul
Journal:
Forensic science international
Issue:
Volume 22(2016:May)
Page Start:
e7
Record Type:
Journal Article
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2. Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. Issue 11 (November 2018)

Authors:
Liaqat, Khurram; Chiu, Ilene; Lee, Kwanghyuk; Chakchouk, Imen; Andrade-Elizondo, Paula; Santos-Cortez, Regie; Hussain, Shabir; Nawaz, Shoaib; Ansar, Muhammad; Khan, Muhammad; Basit, Sulman; Schrauwen, Isabelle; Ahmad, Wasim; Leal, Suzanne
Journal:
Journal of human genetics
Issue:
Volume 63:Issue 11(2018)
Page Start:
1099
Record Type:
Journal Article
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3. Narrow‐wide‐row planting pattern increases the radiation use efficiency and seed yield of intercrop species in relay‐intercropping system. (18th May 2019)

Authors:
Raza, Muhammad Ali; Feng, Ling Yang; van der Werf, Wopke; Cai, Gao Ren; Khalid, Muhammad Hayder Bin; Iqbal, Nasir; Hassan, Muhammad Jawad; Meraj, Tehseen Ahmad; Naeem, Muhammd; Khan, Imran; Rehman, Sana ur; Ansar, Muhammad; Ahmed, Mukhtar; Yang, Feng; Yang, Wenyu
Journal:
Food and energy security
Issue:
Volume 8:Number 3(2019)
Page Start:
n/a
Record Type:
Journal Article
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4. Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3. (16th May 2018)

Authors:
Ansar, Muhammad; Chung, Hyunglok; Waryah, Yar M; Makrythanasis, Periklis; Falconnet, Emilie; Rao, Ali Raza; Guipponi, Michel; Narsani, Ashok K; Fingerhut, Ralph; Santoni, Federico A; Ranza, Emmanuelle; Waryah, Ali M; Bellen, Hugo J; Antonarakis, Stylianos E
Journal:
Human molecular genetics
Issue:
Volume 27:Number 15(2018:Aug. 01)
Page Start:
2703
Record Type:
Journal Article
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5. Genetic analysis of consanguineous families presenting with congenital ocular defects. (May 2016)

Authors:
Ullah, Ehsan; Nadeem Saqib, Muhammad Arif; Sajid, Sundus; Shah, Neelam; Zubair, Muhammad; Khan, Muzammil Ahmad; Ahmed, Iftikhar; Ali, Ghazanfar; Dutta, Atanu Kumar; Danda, Sumita; Lao, Richard; Ling-Fung Tang, Paul; Kwok, Pui-yan; Ansar, Muhammad; Slavotinek, Anne
Journal:
Experimental eye research
Issue:
Volume 146(2016:May)
Page Start:
163
Record Type:
Journal Article
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8. Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix. Issue 3 (13th December 2016)

Authors:
Shah, Khadim; Ansar, Muhammad; Mughal, Zaib-un-Nisa; Khan, Falak Sher; Ahmad, Wasim; Ferrara, Tracey M; Spritz, Richard A
Journal:
Journal of medical genetics
Issue:
Volume 54:Issue 3(2017)
Page Start:
186
Record Type:
Journal Article
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9. 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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