Defining the Need for Genetic Stock Assignment when Describing Stock Demographics and Dynamics: an Example using Lake Whitefish in Lake Michigan von Isermann, Daniel A., Belnap, Matthew J., Turnquist, Keith N., Sloss, Brian L., VanDeHey, Justin A., Hansen, Scott P., Caroffino, David C.

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Loss of foundation species increases population growth of exotic forbs in sagebrush steppe von Prevéy, Janet S, Germino, Matthew J, Huntly, Nancy J

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Conditional vulnerability of plant diversity to atmospheric nitrogen deposition across the United States von Simkin, Samuel M., Allen, Edith B., Bowman, William D., Clark, Christopher M., Belnap, Jayne, Brooks, Matthew L., Cade, Brian S., Collins, Scott L., Geiser, Linda H., Gilliam, Frank S., Jovan, Sarah E., Pardo, Linda H., Schulz, Bethany K., Stevens, Carly J., Suding, Katharine N., Throop, Heather L., Waller, Donald M.

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What is a biocrust? A refined, contemporary definition for a broadening research community von Weber, Bettina, Belnap, Jayne, Büdel, Burkhard, Antoninka, Anita J., Barger, Nichole N., Chaudhary, V. Bala, Darrouzet‐Nardi, Anthony, Eldridge, David J., Faist, Akasha M., Ferrenberg, Scott, Havrilla, Caroline A., Huber‐Sannwald, Elisabeth, Malam Issa, Oumarou, Maestre, Fernando T., Reed, Sasha C., Rodriguez‐Caballero, Emilio, Tucker, Colin, Young, Kristina E., Zhang, Yuanming, Zhao, Yunge, Zhou, Xiaobing, Bowker, Matthew A.

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The pervasive and multifaceted influence of biocrusts on water in the world's drylands von Eldridge, David J., Reed, Sasha, Travers, Samantha K., Bowker, Matthew A., Maestre, Fernando T., Ding, Jingyi, Havrilla, Caroline, Rodriguez‐Caballero, Emilio, Barger, Nichole, Weber, Bettina, Antoninka, Anita, Belnap, Jayne, Chaudhary, Bala, Faist, Akasha, Ferrenberg, Scott, Huber‐Sannwald, Elisabeth, Malam Issa, Oumarou, Zhao, Yunge

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Responses of biological soil crusts to rehabilitation strategies von Chock, Taylor, Antoninka, Anita J., Faist, Akasha M., Bowker, Matthew A., Belnap, Jayne, Barger, Nichole N.

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Towards a predictive framework for biocrust mediation of plant performance: A meta‐analysis von Havrilla, Caroline A., Chaudhary, V. Bala, Ferrenberg, Scott, Antoninka, Anita J., Belnap, Jayne, Bowker, Matthew A., Eldridge, David J., Faist, Akasha M., Huber‐Sannwald, Elisabeth, Leslie, Alexander D., Rodriguez‐Caballero, Emilio, Zhang, Yuanming, Barger, Nichole N., Vries, Franciska

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Sequence and Structural Characterization of Great Salt Lake Bacteriophage CW02, a Member of the T7-Like Supergroup von SHEN, Peter S, DOMEK, Matthew J, BELNAP, David M, SANZ-GARCIA, Eduardo, MAKAJU, Aman, TAYLOR, Ryan M, HOGGAN, Ryan, CULUMBER, Michele D, OBERG, Craig J, BREAKWELL, Donald P, PRINCE, John T

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Correlates of Biological Soil Crust Abundance across a Continuum of Spatial Scales: Support for a Hierarchical Conceptual Model von Bowker, Matthew A., Belnap, Jayne, Davidson, Diane W., Goldstein, Harland

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Inoculation and habitat amelioration efforts in biological soil crust recovery vary by desert and soil texture von Faist, Akasha M., Antoninka, Anita J., Belnap, Jayne, Bowker, Matthew A., Duniway, Michael C., Garcia‐Pichel, Ferran, Nelson, Corey, Reed, Sasha C., Giraldo‐Silva, Ana, Velasco‐Ayuso, Sergio, Barger, Nichole N.

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Inherited CSNK2A1 variants in families with Okur‐Chung neurodevelopmental syndrome von Belnap, Newell, Price‐Smith, Aiai, Ramsey, Keri, Leka, Kamawela, Abraham, Anna, Lieberman, Emma, Hassett, Katie, Potu, Sai, Rudy, Natasha, Smith, Kirstin, Mikhail, Fady M., Monaghan, Kirstin G., Hendershot, Andrea, Mourmans, Jeroen, Descartes, Maria, Huentelman, Matthew J., Sills, Jennifer, Rangasamy, Sampath, Narayanan, Vinodh

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Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant von Leung, Megumi, Sanchez-Castillo, Meredith, Belnap, Newell, Naymik, Marcus, Bonfitto, Anna, Sloan, Jennifer, Hassett, Katie, Jepsen, Wayne M., Sankaramoorthy, Aravind, Stewart, Tracy Murray, Foley, Jackson R., Rangasamy, Sampathkumar, Huentelman, Matthew J., Narayanan, Vinodh, Ramsey, Keri

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Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish von Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N., Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L., Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R., Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N., Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, De Jonghe, Peter

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Preamputation Mirror Therapy May Prevent Development of Phantom Limb Pain: A Case Series von Hanling, Steven R., Wallace, Scott C., Hollenbeck, Kerry J., Belnap, Brian D., Tulis, Matthew R.

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Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders von Frankel, Eric, Podder, Avijit, Sharifi, Megan, Pillai, Roshan, Belnap, Newell, Ramsey, Keri, Dodson, Julius, Venugopal, Pooja, Brzezinski, Molly, Llaci, Lorida, Gerald, Brittany, Mills, Gabrielle, Sanchez-Castillo, Meredith, Balak, Chris D, Szelinger, Szabolcs, Jepsen, Wayne M, Siniard, Ashley L, Richholt, Ryan, Naymik, Marcus, Schrauwen, Isabelle, Craig, David W, Piras, Ignazio S, Huentelman, Matthew J, Schork, Nicholas J, Narayanan, Vinodh, Rangasamy, Sampathkumar

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Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results von Gerald, Brittany, Ramsey, Keri, Belnap, Newell, Szelinger, Szabolcs, Siniard, Ashley L., Balak, Chris, Russell, Megan, Richholt, Ryan, De Both, Matt, Claasen, Ana M., Schrauwen, Isabelle, Huentelman, Matthew J., Craig, David W., Rangasamy, Sampathkumar, Narayanan, Vinodh

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Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD) von Llaci, Lorida, Ramsey, Keri, Belnap, Newell, Claasen, Ana M., Balak, Chris D., Szelinger, Szabolcs, Jepsen, Wayne M., Siniard, Ashley L., Richholt, Ryan, Izat, Tyler, Naymik, Marcus, De Both, Matt, Piras, Ignazio S., Craig, David W., Huentelman, Matthew J., Narayanan, Vinodh, Schrauwen, Isabelle, Rangasamy, Sampathkumar

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Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2 von Jepsen, Wayne M., Ramsey, Keri, Szelinger, Szabolcs, Llaci, Lorida, Balak, Chris, Belnap, Newell, Bilagody, Cherae, De Both, Matthew, Gupta, Raj, Naymik, Marcus, Pandey, Richa, Piras, Ignazio S., Sanchez‐Castillo, Meredith, Rangasamy, Sampathkumar, Narayanan, Vinodh, Huentelman, Matthew J.

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Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilit... von Banuelos, Erika, Ramsey, Keri, Belnap, Newell, Krishnan, Malavika, Balak, Chris, Szelinger, Szabolcs, Siniard, Ashley L, Russell, Megan, Richholt, Ryan, De Both, Matt, Piras, Ignazio, Naymik, Marcus, Claasen, Ana M, Rangasamy, Sampathkumar, Huentelman, Matthew J, Craig, David W, Campeau, Philippe M, Narayanan, Vinodh, Schrauwen, Isabelle

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Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations von Ramsey, Keri, Belnap, Newell, Bonfitto, Anna, Jepsen, Wayne, Naymik, Marcus, Sanchez‐Castillo, Meredith, Craig, David W., Szelinger, Szabolcs, Huentelman, Matthew J., Narayanan, Vinodh, Rangasamy, Sampath

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