Case Report: Development of Factor VIII Inhibitor in a Patient with an Uncommon de novo Mutation in the Factor VIII Gene von Wyatt, Kirk D., Coon, Lea M., Rusk, Dawn N., Rodriguez, Vilmarie, Warad, Deepti M.

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Genotype–phenotype correlation of hereditary erythrocytosis mutations, a single center experience von Oliveira, Jennifer L., Coon, Lea M., Frederick, Lori A., Hein, Molly, Swanson, Kenneth C., Savedra, Michelle E., Porter, Tavanna R., Patnaik, Mrinal M., Tefferi, Ayalew, Pardanani, Animesh, Grebe, Stefan K., Viswanatha, David S., Hoyer, James D.

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Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant von Han, Chen G., O'Brien, Kevin J., Coon, Lea M., Majerus, Julie A., Huryn, Laryssa A., Haroutunian, Sara G., Moka, Nagabhishek, Introne, Wendy J., Macnamara, Ellen, Gahl, William A., Malicdan, May Christine V., Chen, Dong, Krishnan, Koyamangalath, Gochuico, Bernadette R.

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Practice patterns in the diagnosis of inherited platelet disorders within a single institution von Perez Botero, Juliana, Pruthi, Rajiv K, Majerus, Julie A, Coon, Lea M, Uhl, Cindy B, Chen, Dong, Patnaik, Mrinal M

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An Erythrocytosis-Associated Mutation in the Zinc Finger of PHD2 Provides Insights into Its Binding of p23 von Song, Daisheng, Guan, Wei, Coon, Lea M, Al-Kali, Aref, Oliveira, Jennifer L, Lee, Frank S

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Spectrum of Mutations Associated with Hereditary Erythrocytosis von Oliveira, Jennifer L, Frederick, Lori A, Coon, Lea M, Hein, Molly Susan, Patnaik, Mrinal M, Tefferi, Ayalew, Pardanani, Animesh, Grebe, Stefan K, Viswanatha, David S, Hoyer, James D

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Deletional HPFH Vs. Delta Beta Thalassemia: Closing in on a Possible Hb F Silencer Location von Hein, Molly Susan, Swanson, Kenneth C, Lundquist, Patrick A, Yungerberg, Joella A, Coon, Lea M, Dawson, Brian D, Jevremovic, Dragan, Oliveira, Andre M, Hoyer, James D, Oliveira, Jennifer L

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Large Deletions Involving the Beta Globin Gene Complex: Genotype-Phenotype Correlation of 119 Cases von Hein, Molly Susan, Oliveira, Jennifer L, Swanson, Kenneth C, Lundquist, Patrick A, Yungerberg, Joella A, Coon, Lea M, Dawson, Brian D, Go, Ronald S., Jevremovic, Dragan, Hoyer, James D

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Fast and deep phosphoproteome analysis with the Orbitrap Astral mass spectrometer von Lancaster, Noah M., Sinitcyn, Pavel, Forny, Patrick, Peters-Clarke, Trenton M., Fecher, Caroline, Smith, Andrew J., Shishkova, Evgenia, Arrey, Tabiwang N., Pashkova, Anna, Robinson, Margaret Lea, Arp, Nicholas, Fan, Jing, Hansen, Juli, Galmozzi, Andrea, Serrano, Lia R., Rojas, Julie, Gasch, Audrey P., Westphall, Michael S., Stewart, Hamish, Hock, Christian, Damoc, Eugen, Pagliarini, David J., Zabrouskov, Vlad, Coon, Joshua J.

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The One Hour Human Proteome von Serrano, Lia R., Peters-Clarke, Trenton M., Arrey, Tabiwang N., Damoc, Eugen, Robinson, Margaret Lea, Lancaster, Noah M., Shishkova, Evgenia, Moss, Corinne, Pashkova, Anna, Sinitcyn, Pavel, Brademan, Dain R., Quarmby, Scott T., Peterson, Amelia C., Zeller, Martin, Hermanson, Daniel, Stewart, Hamish, Hock, Christian, Makarov, Alexander, Zabrouskov, Vlad, Coon, Joshua J.

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Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p von Weiner, Daniel J., Ling, Emi, Erdin, Serkan, Tai, Derek J. C., Yadav, Rachita, Grove, Jakob, Fu, Jack M., Nadig, Ajay, Carey, Caitlin E., Baya, Nikolas, Bybjerg-Grauholm, Jonas, Berretta, Sabina, Macosko, Evan Z., Sebat, Jonathan, O’Connor, Luke J., Hougaard, David M., Børglum, Anders D., Talkowski, Michael E., McCarroll, Steven A., Robinson, Elise B.

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Comparison of αLEPRA and αLELY Co-Inheritance with a SPTA1 Whole Gene Deletion, a Family Study von Hein, Molly S., Coon, Lea, Porter, Tavanna R., He, Rong, Savedra, Michelle E., Train, Laura J., Baudhuin, Linnea M., Oliveira, Andre M., Nguyen, Phuong L., Hoyer, James D., Rangan, Aruna, Oliveira, Jennifer L.

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