The Diagnosis of Acute Mesenteric Ischemia: A Systematic Review and Meta‐analysis von Cudnik, Michael T., Darbha, Subrahmanyam, Jones, Janice, Macedo, Julian, Stockton, Sherrill W., Hiestand, Brian C., Jones, Alan E.

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Thrombotic risk in congenital erythrocytosis due to up-regulated hypoxia sensing is not associated with elevated hematocrit von Gordeuk, Victor R, Miasnikova, Galina Y, Sergueeva, Adelina I, Lorenzo, Felipe R, Zhang, Xu, Song, Jihyun, Stockton, David W, Prchal, Josef T

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Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia von Ang, Sonny O., Chen, Hua, Hirota, Kiichi, Gordeuk, Victor R., Jelinek, Jaroslav, Guan, Yongli, Liu, Enli, Sergueeva, Adelina I., Miasnikova, Galina Y., Mole, David, Maxwell, Patrick H., Stockton, David W., Semenza, Gregg L., Prchal, Josef T.

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Molecular-Level Processing of Conjugated Polymers. 4. Layer-by-Layer Manipulation of Polyaniline via Hydrogen-Bonding Interactions von Stockton, W. B, Rubner, M. F

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An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions von Kim, Bum Jun, Zaveri, Hitisha P, Shchelochkov, Oleg A, Yu, Zhiyin, Hernández-García, Andrés, Seymour, Michelle L, Oghalai, John S, Pereira, Fred A, Stockton, David W, Justice, Monica J, Lee, Brendan, Scott, Daryl A

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Mucopolysaccharidosis Type I Newborn Screening: Best Practices for Diagnosis and Management von Clarke, Lorne A., MD, CM, FRCPC, FCCMG, Atherton, Andrea M., MS, CGC, Burton, Barbara K., MD, FAAP, FACMG, Day-Salvatore, Debra L., MD, PhD, FAAP, FACMG, Kaplan, Paige, MBBCh, FRCPC, FCCMG, FAAP, FACMG, Leslie, Nancy D., MD, Scott, C. Ronald, MD, Stockton, David W., MD, FACMG, Thomas, Janet A., MD, FAAP, FACMG, Muenzer, Joseph, MD, PhD

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Mutation of PAX9 is associated with oligodontia von Stockton, David W., Das, Parimal, Goldenberg, Monica, D'Souza, Rena N., Patel, Pragna I.

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Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity von Bachmann-Gagescu, Ruxandra, Mefford, Heather C., Cowan, Charles, Glew, Gwen M., Hing, Anne V., Wallace, Stephanie, Bader, Patricia I., Hamati, Aline, Reitnauer, Pamela J., Smith, Rosemarie, Stockton, David W., Muhle, Hiltrud, Helbig, Ingo, Eichler, Evan E., Ballif, Blake C., Rosenfeld, Jill, Tsuchiya, Karen D.

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Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy von Takashima, Hiroshi, Boerkoel, Cornelius F., John, Joy, Saifi, Gulam Mustafa, Salih, Mustafa A.M., Armstrong, Dawna, Mao, Yuxin, Quiocho, Florante A., Roa, Benjamin B., Nakagawa, Masanori, Stockton, David W., Lupski, James R.

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Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy von Sen, Kuntal, Kaur, Shagun, Stockton, David W., Nyhuis, Mary, Roberson, Jacquelyn

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Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C von Nowakowska, Beata A., Obersztyn, Ewa, Szymańska, Krystyna, Bekiesińska-Figatowska, Monika, Xia, Zhilian, Ricks, Christian B., Bocian, Ewa, Stockton, David W., Szczałuba, Krzysztof, Nawara, Magdalena, Patel, Ankita, Scott, Daryl A., Cheung, Sau Wai, Bohan, Timothy P., Stankiewicz, Paweł

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Expanding the phenotype of alveolar capillary dysplasia (ACD) von Sen, Partha, Thakur, Nivedita, Stockton, David W., Langston, Claire, Bejjani, Bassem A.

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Can Functional Polymorphisms in VEGF and MMP Predict Intraventricular Hemorrhage in Extremely Preterm Newborns? von Prasun, Pankaj, Madan, Raghav, Puthuraya, Subhash, Subramanian, Divya, Datta, Ishita, Kalra, Vaneet, Thomas, Ronald, Stockton, David W., Sundaram, Senthil, Callaghan, Joseph, Callaghan, Michael, Chouthai, Nitin

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Reconstruction of the North Atlantic Oscillation, 1429–1983 von Glueck, Mary F., Stockton, Charles W.

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Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease von Kralovics, Robert, Stockton, David W., Prchal, Josef T.

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Molecular-Level Processing of Conjugated Polymers. 3. Layer-by-Layer Manipulation of Polyaniline via Electrostatic Interactions von Cheung, J. H, Stockton, W. B, Rubner, M. F

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Functional genetic analysis of mouse chromosome 11 von Kile, Benjamin T., Hentges, Kathryn E., Clark, Amander T., Nakamura, Hisashi, Salinger, Andrew P., Liu, Bin, Box, Neil, Stockton, David W., Johnson, Randy L., Behringer, Richard R., Bradley, Allan, Justice, Monica J.

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Metabonomics classifies pathways affected by bioactive compounds. Artificial neural network classification of NMR spectra of plant extracts von Ott, Karl-Heinz, Aranı&#x0301, bar, Nelly, Singh, Bijay, Stockton, Gerald W.

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Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3 von Beck, Tyler F, Shchelochkov, Oleg A, Yu, Zhiyin, Kim, Bum Jun, Hernández-García, Andrés, Zaveri, Hitisha P, Bishop, Colin, Overbeek, Paul A, Stockton, David W, Justice, Monica J, Scott, Daryl A

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Management of COVID‐19 infection in organic acidemias von Kaur, Shagun, Campbell, Stephanie L., Stockton, David W.

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