Chromium: celebrating 50 years as an essential element?
Vincent, John B
Published in Dalton transactions : an international journal of inorganic chemistry (01.01.2010)
Published in Dalton transactions : an international journal of inorganic chemistry (01.01.2010)
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Journal Article
Bears Show a Physiological but Limited Behavioral Response to Unmanned Aerial Vehicles
Ditmer, Mark A., Vincent, John B., Werden, Leland K., Tanner, Jessie C., Laske, Timothy G., Iaizzo, Paul A., Garshelis, David L., Fieberg, John R.
Published in Current biology (31.08.2015)
Published in Current biology (31.08.2015)
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Journal Article
Ectomycorrhizal fungal diversity and saprotrophic fungal diversity are linked to different tree community attributes in a field-based tree experiment
Nguyen, Nhu H., Williams, Laura J., Vincent, John B., Stefanski, Artur, Cavender-Bares, Jeannine, Messier, Christian, Paquette, Alain, Gravel, Dominique, Reich, Peter B., Kennedy, Peter G.
Published in Molecular ecology (01.08.2016)
Published in Molecular ecology (01.08.2016)
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Journal Article
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
Khan, Muzammil Ahmad, Rafiq, Muhammad Arshad, Noor, Abdul, Hussain, Shobbir, Flores, Joana V., Rupp, Verena, Vincent, Akshita K., Malli, Roland, Ali, Ghazanfar, Khan, Falak Sher, Ishak, Gisele E., Doherty, Dan, Weksberg, Rosanna, Ayub, Muhammad, Windpassinger, Christian, Ibrahim, Shahnaz, Frye, Michaela, Ansar, Muhammad, Vincent, John B.
Published in American journal of human genetics (04.05.2012)
Published in American journal of human genetics (04.05.2012)
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Journal Article
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
Johansen, Anide, Rosti, Rasim O., Musaev, Damir, Sticca, Evan, Harripaul, Ricardo, Zaki, Maha, Çağlayan, Ahmet Okay, Azam, Matloob, Sultan, Tipu, Froukh, Tawfiq, Reis, André, Popp, Bernt, Ahmed, Iltaf, John, Peter, Ayub, Muhammad, Ben-Omran, Tawfeg, Vincent, John B., Gleeson, Joseph G., Abou Jamra, Rami
Published in American journal of human genetics (06.10.2016)
Published in American journal of human genetics (06.10.2016)
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Journal Article
Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder
Khan, Hamid, Harripaul, Ricardo, Mikhailov, Anna, Herzi, Sumayah, Bowers, Sonya, Ayub, Muhammad, Shabbir, Muhammad Imran, Vincent, John B.
Published in Scientific reports (22.04.2024)
Published in Scientific reports (22.04.2024)
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Journal Article
The genetic basis of non-syndromic intellectual disability: a review
Kaufman, Liana, Ayub, Muhammad, Vincent, John B
Published in Journal of neurodevelopmental disorders (01.12.2010)
Published in Journal of neurodevelopmental disorders (01.12.2010)
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Journal Article
Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
Law, Rosalind, Dixon-Salazar, Tracy, Jerber, Julie, Cai, Na, Abbasi, Ansar A., Zaki, Maha S., Mittal, Kirti, Gabriel, Stacey B., Rafiq, Muhammad Arshad, Khan, Valeed, Nguyen, Maria, Ali, Ghazanfar, Copeland, Brett, Scott, Eric, Vasli, Nasim, Mikhailov, Anna, Khan, Muhammad Nasim, Andrade, Danielle M., Ayaz, Muhammad, Ansar, Muhammad, Ayub, Muhammad, Vincent, John B., Gleeson, Joseph G.
Published in American journal of human genetics (04.12.2014)
Published in American journal of human genetics (04.12.2014)
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Journal Article
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family
Khan, Muzammil A, Rupp, Verena M, Orpinell, Meritxell, Hussain, Muhammad S, Altmüller, Janine, Steinmetz, Michel O, Enzinger, Christian, Thiele, Holger, Höhne, Wolfgang, Nürnberg, Gudrun, Baig, Shahid M, Ansar, Muhammad, Nürnberg, Peter, Vincent, John B, Speicher, Michael R, Gönczy, Pierre, Windpassinger, Christian
Published in Human molecular genetics (15.11.2014)
Published in Human molecular genetics (15.11.2014)
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Journal Article
Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14
Pastore, Stephen F., Muhammad, Tahir, Harripaul, Ricardo, Lau, Rebecca, Khan, Muhammad Tariq Masood, Khan, Muhammad Ismail, Islam, Omar, Kang, Changsoo, Ayub, Muhammad, Jelani, Musharraf, Vincent, John B.
Published in Scientific reports (30.11.2021)
Published in Scientific reports (30.11.2021)
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Journal Article
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families
Egger, Gerald, Roetzer, Katharina M., Noor, Abdul, Lionel, Anath C., Mahmood, Huda, Schwarzbraun, Thomas, Boright, Oliver, Mikhailov, Anna, Marshall, Christian R., Windpassinger, Christian, Petek, Erwin, Scherer, Stephen W., Kaschnitz, Wolfgang, Vincent, John B.
Published in Neurogenetics (01.05.2014)
Published in Neurogenetics (01.05.2014)
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