Error Bounds on the SCISSORS Approximation Method

Por Haque, Imran S., Pande, Vijay S.
Publicado em 2011

SIML: A Fast SIMD Algorithm for Calculating LINGO Chemical Similarities on GPUs and CPUs

Por Haque, Imran S., Pande, Vijay S., Walters, W. Patrick
Publicado em 2010

SCISSORS: Practical Considerations

Por Kearnes, Steven M., Haque, Imran S., Pande, Vijay S.
Publicado em 2013

The Anatomy of High-Performance 2D Similarity Calculations

Por Haque, Imran S., Pande, Vijay S., Walters, W. Patrick
Publicado no J Chem Inf Model (2011)

Response to Stoll and Resta

Por Lazarin, Gabriel A., Haque, Imran S., Nazareth, Shivani, Evans, Eric A.
Publicado em 2013

Smith–Lemli–Opitz syndrome carrier frequency and estimates of in utero mortality rates

Por Lazarin, Gabriel A., Haque, Imran S., Evans, Eric A., Goldberg, James D.
Publicado no Prenat Diagn (2017)

MSMBuilder2: Modeling Conformational Dynamics at the Picosecond to Millisecond Scale

Por Beauchamp, Kyle A., Bowman, Gregory R., Lane, Thomas J., Maibaum, Lutz, Haque, Imran S., Pande, Vijay S.
Publicado em 2011

Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels

Por Lazarin, Gabriel A., Hawthorne, Felicia, Collins, Nicholas S., Platt, Elizabeth A., Evans, Eric A., Haque, Imran S.
Publicado no PLoS One (2014)

Tay-Sachs Carrier Screening by Enzyme and Molecular Analyses in the New York City Minority Population

Por Mehta, Nikita, Lazarin, Gabriel A., Spiegel, Erica, Berentsen, Kathleen, Brennan, Kelly, Giordano, Jessica, Haque, Imran S., Wapner, Ronald
Publicado no Genet Test Mol Biomarkers (2016)

Clinical and histopathologic characteristics of skin malignancies in Qassim Region, Saudi Arabia

Por Alzolibani, Abdullateef A., Al Shobaili, Hani A., Robaee, Ahmad Al, Khan, Athar, Haque, Imran Ul, Rao, Nagendra Seethapathi, Alrejaie, Abdulaziz
Publicado em 2013

The population genetics of human disease: The case of recessive, lethal mutations

Por Amorim, Carlos Eduardo G., Gao, Ziyue, Baker, Zachary, Diesel, José Francisco, Simons, Yuval B., Haque, Imran S., Pickrell, Joseph, Przeworski, Molly
Publicado no PLoS Genet (2017)

Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing

Por Kang, Hyunseok P., Maguire, Jared R., Chu, Clement S., Haque, Imran S., Lai, Henry, Mar-Heyming, Rebecca, Ready, Kaylene, Vysotskaia, Valentina S., Evans, Eric A.
Publicado no PeerJ (2016)

An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals

Por Lazarin, Gabriel A., Haque, Imran S., Nazareth, Shivani, Iori, Kevin, Patterson, A. Scott, Jacobson, Jessica L., Marshall, John R., Seltzer, William K., Patrizio, Pasquale, Evans, Eric A., Srinivasan, Balaji S.
Publicado em 2013

Systematic design and comparison of expanded carrier screening panels

Por Beauchamp, Kyle A, Muzzey, Dale, Wong, Kenny K, Hogan, Gregory J, Karimi, Kambiz, Candille, Sophie I, Mehta, Nikita, Mar-Heyming, Rebecca, Kaseniit, K Eerik, Kang, H Peter, Evans, Eric A, Goldberg, James D, Lazarin, Gabriel A, Haque, Imran S
Publicado no Genet Med (2018)

Current Status of the AMOEBA Polarizable Force Field

Por Ponder, Jay W., Wu, Chuanjie, Ren, Pengyu, Pande, Vijay S., Chodera, John D., Schnieders, Michael J., Haque, Imran, Mobley, David L., Lambrecht, Daniel S., DiStasio, Robert A., Head-Gordon, Martin, Clark, Gary N. I., Johnson, Margaret E., Head-Gordon, Teresa
Publicado em 2010

Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment

Por Vysotskaia, Valentina S., Hogan, Gregory J., Gould, Genevieve M., Wang, Xin, Robertson, Alex D., Haas, Kevin R., Theilmann, Mark R., Spurka, Lindsay, Grauman, Peter V., Lai, Henry H., Jeon, Diana, Haliburton, Genevieve, Leggett, Matt, Chu, Clement S., Iori, Kevin, Maguire, Jared R., Ready, Kaylene, Evans, Eric A., Kang, Hyunseok P., Haque, Imran S.
Publicado no PeerJ (2017)