Current and future perspectives of liquid biopsies in genomics-driven oncology von Heitzer, Ellen, Haque, Imran S., Roberts, Charles E. S., Speicher, Michael R.

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Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels von Lazarin, Gabriel A, Hawthorne, Felicia, Collins, Nicholas S, Platt, Elizabeth A, Evans, Eric A, Haque, Imran S

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The population genetics of human disease: The case of recessive, lethal mutations von Amorim, Carlos Eduardo G, Gao, Ziyue, Baker, Zachary, Diesel, José Francisco, Simons, Yuval B, Haque, Imran S, Pickrell, Joseph, Przeworski, Molly

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Modeled Fetal Risk of Genetic Diseases Identified by Expanded Carrier Screening von Haque, Imran S, Lazarin, Gabriel A, Kang, H. Peter, Evans, Eric A, Goldberg, James D, Wapner, Ronald J

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Genetic ancestry analysis on >93,000 individuals undergoing expanded carrier screening reveals limitations of ethnicity-based medical guidelines von Kaseniit, Kristjan E., Haque, Imran S., Goldberg, James D., Shulman, Lee P., Muzzey, Dale

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Machine learning enables detection of early-stage colorectal cancer by whole-genome sequencing of plasma cell-free DNA von Wan, Nathan, Weinberg, David, Liu, Tzu-Yu, Niehaus, Katherine, Ariazi, Eric A, Delubac, Daniel, Kannan, Ajay, White, Brandon, Bailey, Mitch, Bertin, Marvin, Boley, Nathan, Bowen, Derek, Cregg, James, Drake, Adam M, Ennis, Riley, Fransen, Signe, Gafni, Erik, Hansen, Loren, Liu, Yaping, Otte, Gabriel L, Pecson, Jennifer, Rice, Brandon, Sanderson, Gabriel E, Sharma, Aarushi, St John, John, Tang, Catherina, Tzou, Abraham, Young, Leilani, Putcha, Girish, Haque, Imran S

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Expanded carrier screening: A review of early implementation and literature von Lazarin, Gabriel A., MS, Haque, Imran S., PhD

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MSMBuilder2: Modeling Conformational Dynamics on the Picosecond to Millisecond Scale von Beauchamp, Kyle A, Bowman, Gregory R, Lane, Thomas J, Maibaum, Lutz, Haque, Imran S, Pande, Vijay S

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Enhanced DNA libraries for methylation analysis von Haque, Imran S.

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Current Status of the AMOEBA Polarizable Force Field von 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

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High-resolution genome-wide mapping of chromosome-arm-scale truncations induced by CRISPR–Cas9 editing von Lazar, Nathan H., Celik, Safiye, Chen, Lu, Fay, Marta M., Irish, Jonathan C., Jensen, James, Tillinghast, Conor A., Urbanik, John, Bone, William P., Gibson, Christopher C., Haque, Imran S.

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Building, benchmarking, and exploring perturbative maps of transcriptional and morphological data von Celik, Safiye, Hütter, Jan-Christian, Carlos, Sandra Melo, Lazar, Nathan H, Mohan, Rahul, Tillinghast, Conor, Biancalani, Tommaso, Fay, Marta M, Earnshaw, Berton A, Haque, Imran S

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

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Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples von Ghiossi, Caroline E., Goldberg, James D., Haque, Imran S., Lazarin, Gabriel A., Wong, Kenny K.

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Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification von Hogan, Gregory J, Vysotskaia, Valentina S, Beauchamp, Kyle A, Seisenberger, Stefanie, Grauman, Peter V, Haas, Kevin R, Hong, Sun Hae, Jeon, Diana, Kash, Shera, Lai, Henry H, Melroy, Laura M, Theilmann, Mark R, Chu, Clement S, Iori, Kevin, Maguire, Jared R, Evans, Eric A, Haque, Imran S, Mar-Heyming, Rebecca, Kang, Hyunseok P, Muzzey, Dale

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Smith–Lemli–Opitz syndrome carrier frequency and estimates of in utero mortality rates von Lazarin, Gabriel A., Haque, Imran S., Evans, Eric A., Goldberg, James D.

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Knowledge and attitudes regarding expanded genetic carrier screening among women’s healthcare providers von Ready, Kaylene, M.S, Haque, Imran S., Ph.D, Srinivasan, Balaji S., Ph.D, Marshall, John R., M.D

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Systematic design and comparison of expanded carrier screening panels von 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.

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Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods von Artieri, Carlo G., Haverty, Carrie, Evans, Eric A., Goldberg, James D., Haque, Imran S., Yaron, Yuval, Muzzey, Dale

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Prenatal Carrier Screening von Haque, Imran S, Lazarin, Gabriel A, Wapner, Ronald J

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