Urogenital Infections as a Risk Factor for Preterm Labor: A Hospital-Based Case–Control Study von Verma, Indu, Avasthi, Kumkum, Berry, Vandana

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Bacterial biofilm formation, pathogenicity, diagnostics and control: An overview von Sawhney, Rajesh, Berry, Vandana

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia von Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome von Lewandowski, Kathryn Eve, Shashi, Vandana, Berry, Peggy M., Kwapil, Thomas R.

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The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome von Shashi, V., Xie, P., Schoch, K., Goldstein, D.B., Howard, T.D., Berry, M.N., Schwartz, C.E., Cronin, K., Sliwa, S., Allen, A., Need, A.C.

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COVID-19 trajectories among 57 million adults in England: a cohort study using electronic health records von Thygesen, Johan H, Mizani, Mehrdad A, Banerjee, Amitava, Cooper, Jennifer, Lai, Alvina G, Sudlow, Cathie, Abbasizanjani, Hoda, Ahmed, Nida, Akbari, Ashley, Allery, Freya, Ashworth, Mark, Bacon, Seb, Ball, Steve, Banerjee, Ami, Berry, Colin, Beveridge, Jennifer, Boyle, Jon, Briffa, Norman, Buch, Maya, Canoy, Dexter, Cheema, Kate, Crallan, Rebecca, Curcin, Vasa, Curry, Gwenetta, Denholm, Rachel, Dennis, John, Denniston, Alastair, Deo, Salil, Dhillon, Baljean, Dong, Tim, Downs, Johnny, Dregan, Alexandru, Elwenspoek, Martha, Falter, Florian, Firth, Joseph, Friebel, Rocco, Gilbert, Ruth, Goldacre, Ben, Goldacre, Raph, Grieco, Luca, Handy, Alex, Hardelid, Pia, Hardy, Flavien, Hemingway, Harry, Herz, Naomi, Heyl, Johannes, Hinchliffe, Rosie, Hippisley-Cox, Julia, Hocaoglu, Mevhibe, Hollings, Sam, Inouye, Mike, Jenkins, David, Kadam, Umesh, Kallis, Costas, Khawaja, Anthony, Killick, Richard, Kinnear, Deborah, Kolamunnage-Dona, Ruwanthi, Kurdi, Amanj, Lai, Alvina, Lambarth, Andrew, Larzjan, Milad Nazarzadeh, Li, Qiuju, Lyons, Ronan, Macleod, Mary Joan, Mamouei, Mohammad, Melville, Craig, Moncusi, Marta Pineda, Morales, Daniel, Morris, Carole, Nicholson, George, Norris, Tom, Oliver, Dominic, Oluyase, Adejoke, Pierotti, Livia, Priedon, Rouven, Proudfoot, Alastair, Roberts, Brian, Rossdale, Jennifer, Samani, Nilesh, Sattar, Naveed, Schwartz, Roy, Seminog, Olena, Sinha, Shubhra, Skrypak, Mirek, Sofat, Reecha, Sun, Luanluan, Suseeladevi, Arun Karthikeyan, Tilston, George, Toit, Clea du, Torabi, Fatemeh, Watkinson, Ruth, Whiteley, William, Williams, Michelle, Williams, Richard, Withnell, Eloise, Wright, Lucy, Wu, Jinge, Wu, Jianhua, Zaccardi, Francesco

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Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype von Scurr, Ingrid, Wilson, Louise, Lees, Melissa, Robertson, Stephen, Kirk, Edwin, Turner, Anne, Morton, John, Kidd, Alexa, Shashi, Vandana, Stanley, Christy, Berry, Margaret, Irvine, Alan D., Goudie, David, Turner, Claire, Brewer, Carole, Smithson, Sarah

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Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome von Shashi, Vandana, Kwapil, Thomas R, Kaczorowski, Jessica, Berry, Margaret N, Santos, Cesar S, Howard, Timothy D, Goradia, Dhruman, Prasad, Konasale, Vaibhav, Diwadkar, Rajarethinam, Rajaprabhakaran, Spence, Edward, Keshavan, Matcheri S

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Comparison of tocilizumab and high-dose methylprednisolone pulse on outcomes in severe corona virus disease-2019: TAME-COVID, a retrospective multicentric study von Kumar, Vipin, Kashyap, Anil, Kaur, Simran, John, Mary, Sibia, Raminderpal, Chopra, Vishal, Singla, Tanvi, Jindal, Jyoti, Sethi, Suman, Chhabra, Sandeep, Berry, Amit, Dhooria, Harmeet, Singh, Akashdeep, Garg, Vikas, Jain, Dinesh, Mahajan, Rajesh, Gautam, Parshotam, Midha, Vandana, Mohan, Bishav

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Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome von Shashi, V, Keshavan, MS, Howard, TD, Berry, MN, Basehore, MJ, Lewandowski, E, Kwapil, TR

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COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome von Shashi, Vandana, Howard, Timothy D, Keshavan, Matcheri S, Kaczorowski, Jessica, Berry, Margaret N, Schoch, Kelly, Spence, Edward J, Kwapil, Thomas R

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Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome von Shashi, Vandana, Muddasani, Srirangam, Santos, Cesar C, Berry, Margaret N, Kwapil, Thomas R, Lewandowski, Eve, Keshavan, Matcheri S

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Vasomotor instability in neonates with chromosome 22q11 deletion syndrome von Shashi, Vandana, Berry, Margaret N., Hines, Michael H.

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A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27 von Shashi, Vandana, Berry, Margaret N., Shoaf, Sarah, Sciote, James J., Goldstein, Donald, Hart, Thomas C.

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Prenatal diagnosis of complete sole trisomy 1q von Pettenati, Mark J., Berry, Margaret, Shashi, Vandana, Hartley Bowen, J., Harper, Margaret

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Serodiagnosis of leishmaniasis with recombinant ORFF antigen von Raj, VS, Ghosh, A, Dole, VS, Madhubala, R, Myler, PJ, Stuart, KD

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Partial duplication of 4q12q13 leads to a mild phenotype von Shashi, Vandana, Berry, Margaret N., Santos, César, Pettenati, Mark J.

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A combination of physical examination and ECG detects the majority of hemodynamically significant heart defects in neonates with Down syndrome von Shashi, Vandana, Berry, Margaret N., Covitz, Wesley

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A further case of choanal atresia in the deletion (9p) syndrome von Shashi, Vandana, Berry, David, Stamper, Tara H., Pettenati, Mark

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