Enhanced differentiation of the mouse oli-neu oligodendroglial cell line using optimized culture conditions von Bey, Guillermo Rodriguez, Padiath, Quasar Saleem

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scMAPA: Identification of cell-type–specific alternative polyadenylation in complex tissues von Bai, Yulong, Qin, Yidi, Fan, Zhenjiang, Morrison, Robert M, Nam, KyongNyon, Zarour, Hassane M, Koldamova, Radosveta, Padiath, Quasar Saleem, Kim, Soyeon, Park, Hyun Jung

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Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects von Werren, Elizabeth A, Rodriguez Bey, Guillermo, Majethia, Purvi, Kaur, Parneet, Patil, Siddaramappa J, Kekatpure, Minal, Afenjar, Alexandra, Qebibo, Leila, Burglen, Lydie, Tomoum, Hoda, Demurger, Florence, Duborg, Christele, Siddiqui, Shahyan, Tsan, Yao-Chang, Abdullah, Uzma, Ali, Zafar, Saadi, Saadia Maryam, Baig, Shahid Mahmood, Houlden, Henry, Maroofian, Reza, Padiath, Quasar Saleem, Bielas, Stephanie L, Shukla, Anju

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Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophy von do Rosario, Michelle C, Bey, Guillermo Rodriguez, Nmezi, Bruce, Liu, Fang, Oranburg, Talia, Cohen, Ana S A, Coffman, Keith A, Brown, Maya R, Kiselyov, Kirill, Waisfisz, Quinten, Flohil, Myrthe T, Siddiqui, Shahyan, Rosenfeld, Jill A, Iglesias, Alejandro, Girisha, Katta Mohan, Wolf, Nicole I, Padiath, Quasar Saleem, Shukla, Anju

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Expanding colonies and expanding repeats von Saleem, Quasar, Muthane, Uday, Verma, Inder C, Brahmachari, Samir K, Jain, Sanjeev

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Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele-Specific Expression von Giorgio, Elisa, Rolyan, Harshvardhan, Kropp, Laura, Chakka, Anish Baswanth, Yatsenko, Svetlana, Gregorio, Eleonora Di, Lacerenza, Daniela, Vaula, Giovanna, Talarico, Flavia, Mandich, Paola, Toro, Camilo, Pierre, Eleonore Eymard, Labauge, Pierre, Capellari, Sabina, Cortelli, Pietro, Vairo, Filippo Pinto, Miguel, Diego, Stubbolo, Danielle, Marques, Lourenco Charles, Gahl, William, Boespflug-Tanguy, Odile, Melberg, Atle, Hassin-Baer, Sharon, Cohen, Oren S., Pjontek, Rastislav, Grau, Armin, Klopstock, Thomas, Fogel, Brent, Meijer, Inge, Rouleau, Guy, Bouchard, Jean-Pierre L., Ganapathiraju, Madhavi, Vanderver, Adeline, Dahl, Niklas, Hobson, Grace, Brusco, Alfredo, Brussino, Alessandro, Padiath, Quasar Saleem

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Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus von Padiath, Quasar Saleem, Srivastava, Achal Kumar, Roy, Sanghmitra, Jain, Satish, Brahmachari, Samir Kumar

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Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele-Specific Expression von Giorgio, Elisa, Rolyan, Harshvardhan, Kropp, Laura, Chakka, Anish Baswanth, Yatsenko, Svetlana, Gregorio, Eleonora Di, Lacerenza, Daniela, Vaula, Giovanna, Talarico, Flavia, Mandich, Paola, Toro, Camilo, Pierre, Eleonore Eymard, Labauge, Pierre, Capellari, Sabina, Cortelli, Pietro, Vairo, Filippo Pinto, Miguel, Diego, Stubbolo, Danielle, Marques, Lourenco Charles, Gahl, William, Boespflug-Tanguy, Odile, Melberg, Atle, Hassin-Baer, Sharon, Cohen, Oren S., Pjontek, Rastislav, Grau, Armin, Klopstock, Thomas, Fogel, Brent, Meijer, Inge, Rouleau, Guy, Bouchard, Jean-Pierre L., Ganapathiraju, Madhavi, Vanderver, Adeline, Dahl, Niklas, Hobson, Grace, Brusco, Alfredo, Brussino, Alessandro, Padiath, Quasar Saleem

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Analysis of LMNB 1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele‐Specific Expression von Giorgio, Elisa, Rolyan, Harshvardhan, Kropp, Laura, Chakka, Anish Baswanth, Yatsenko, Svetlana, Gregorio, Eleonora Di, Lacerenza, Daniela, Vaula, Giovanna, Talarico, Flavia, Mandich, Paola, Toro, Camilo, Pierre, Eleonore Eymard, Labauge, Pierre, Capellari, Sabina, Cortelli, Pietro, Vairo, Filippo Pinto, Miguel, Diego, Stubbolo, Danielle, Marques, Lourenco Charles, Gahl, William, Boespflug‐Tanguy, Odile, Melberg, Atle, Hassin‐Baer, Sharon, Cohen, Oren S., Pjontek, Rastislav, Grau, Armin, Klopstock, Thomas, Fogel, Brent, Meijer, Inge, Rouleau, Guy, Bouchard, Jean‐Pierre L., Ganapathiraju, Madhavi, Vanderver, Adeline, Dahl, Niklas, Hobson, Grace, Brusco, Alfredo, Brussino, Alessandro, Padiath, Quasar Saleem

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Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation von Saleem, Q, Choudhry, S, Mukerji, M, Bashyam, L, Padma, M V, Chakravarthy, A, Maheshwari, M C, Jain, S, Brahmachari, S K

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Glycogen Synthase Kinase 3β as a Likely Target for the Action of Lithium on Circadian Clocks von Padiath, Quasar Saleem, Paranjpe, Dhanashree, Jain, Sanjeev, Sharma, Vijay Kumar

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Chance in our strands? von Padiath, Quasar Saleem, Rao, B Jagadeeshwara

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A nonsense mutation in the synaptogyrin 1 gene in a family with schizophrenia von Verma, Ranjana, Chauhan, Chitra, Saleem, Quasar, Gandhi, Charu, Jain, Sanjeev, Brahmachari, Samir K

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The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humans von SALEEM, Quasar, ANAND, Anuranjan, JAIN, Sanjeev, BRAHMACHARI, Samir K

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Glycogen synthase kinase 3beta as a likely target for the action of lithium on circadian clocks von Padiath, Quasar Saleem, Paranjpe, Dhanashree, Jain, Sanjeev, Sharma, Vijay Kumar

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Glycogen Synthase Kinase 3 as a Likely Target for the Action of Lithium on Circadian Clocks von Padiath, Quasar Saleem, Paranjpe, Dhanashree, Jain, Sanjeev, Sharma, Vijay Kumar

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A clinical study of patients with genetically confirmed Huntington's disease from India von Murgod, Uday A, Saleem, Quasar, Anand, A, Brahmachari, S.K, Jain, Sanjeev, Muthane, Uday B

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Probing the polyglutamine puzzle in neurological disorders von Brahmachari, Samir K, Sharma, Deepak, Sharma, Sunitha, Pasha, Santosh, Sen, Somdatta, Saleem, Quasar

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Variation at the MJD locus in the major psychoses von Saleem, Quasar, Vijayakumar, M., Mutsuddi, Mousumi, Chowdhary, Neerja, Jain, Sanjeev, Brahmachari, Samir K.

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Supporting data for "scMAPA: Identification of Cell-type-specific Alternative Polyadenylation in Complex Tissues" von Yulong, Bai, Yidi, Qin, Zhenjiang, Fan, Robert, Morrison, KyongNyon, Nam, Hassane, Zarour Mohamed, Radosveta, Koldamova, Quasar, Padiath Saleem, Soyeon, Kim, Hyun, Park Jung

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