An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics von Chintalaphani, Sanjog R., Pineda, Sandy S., Deveson, Ira W., Kumar, Kishore R.

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Targeting Mitochondrial Impairment in Parkinson's Disease: Challenges and Opportunities von Prasuhn, Jannik, Davis, Ryan L., Kumar, Kishore R.

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A novel approach to unsupervised pattern discovery in speech using Convolutional Neural Network von R., Kishore Kumar, Sreenivasa Rao, K.

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Myelin protein zero–related autosomal dominant peripheral neuropathy presenting as hereditary neuropathy with liability to pressure palsies von Halliwell, Nicholas F., Kumar, Kishore R., Ng, Karl

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Optimizing Nutrition in Preterm Low Birth Weight Infants-Consensus Summary von Kumar, R Kishore, Singhal, Atul, Vaidya, Umesh, Banerjee, Saswata, Anwar, Fahmina, Rao, Shashidhar

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New insights into the complex role of mitochondria in Parkinson's disease von Grünewald, Anne, Kumar, Kishore R, Sue, Carolyn M

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Informing a value care model: lessons from an integrated adult neurogenomics clinic von McLean, Alison, Tchan, Michel, Devery, Sophie, Smyth, Renee, Shrestha, Rupendra, Kumar, Kishore R., Tomlinson, Susan, Tisch, Stephen, Wu, Kathy H. C.

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Reduced acetylated α-tubulin in SPAST hereditary spastic paraplegia patient PBMCs von Wali, Gautam, Siow, Sue-Faye, Liyanage, Erandhi, Kumar, Kishore R, Mackay-Sim, Alan, Sue, Carolyn M

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Pharmacological rescue of mitochondrial and neuronal defects in SPG7 hereditary spastic paraplegia patient neurons using high throughput assays von Wali, Gautam, Li, Yan, Liyanage, Erandhi, Kumar, Kishore R., Day, Margot L., Sue, Carolyn M.

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Genetics of Parkinson disease and other movement disorders von Kumar, Kishore R, Lohmann, Katja, Klein, Christine

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A robust unsupervised pattern discovery and clustering of speech signals von R, Kishore Kumar, Birla, Lokendra, K, Sreenivasa Rao

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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene von Lohmann, Katja, Wilcox, Robert A., Winkler, Susen, Ramirez, Alfredo, Rakovic, Aleksandar, Park, Jin-Sung, Arns, Björn, Lohnau, Thora, Groen, Justus, Kasten, Meike, Brüggemann, Norbert, Hagenah, Johann, Schmidt, Alexander, Kaiser, Frank J., Kumar, Kishore R., Zschiedrich, Katja, Alvarez-Fischer, Daniel, Altenmüller, Eckart, Ferbert, Andreas, Lang, Anthony E., Münchau, Alexander, Kostic, Vladimir, Simonyan, Kristina, Agzarian, Marc, Ozelius, Laurie J., Langeveld, Antonius P. M., Sue, Carolyn M., Tijssen, Marina A. J., Klein, Christine

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Oxygen for the delivery room respiratory support of moderate‐to‐late preterm infants. An international survey of clinical practice from 21 countries von Sotiropoulos, James X., Kapadia, Vishal, Vento, Maximo, Rabi, Yacov, Saugstad, Ola D., Kumar, R. Kishore, Schmölzer, Georg M., Zhang, Huyan, Yuan, Yuan, Lim, Gina, Kusuda, Satoshi, Arimitsu, Takeshi, Nguyen, Tinh Thu, Kitsommart, Ratchada, Yeo, Kee Thai, Oei, Ju Lee

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Racially equitable diagnosis of cystic fibrosis using next-generation DNA sequencing: a case report von Shum, Bennett O. V., Bennett, Glenn, Navilebasappa, Akash, Kumar, R. Kishore

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New gene implicated in early‐onset generalized dystonia: Lysine‐specific methyltransferase 2B (KMT2B) von Siow, Sue‐Faye, Kumar, Kishore R.

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Motor Evoked Potentials in Hereditary Spastic Paraplegia—A Systematic Review von Siow, Sue-Faye, Cameron Smail, Ruaridh, Ng, Karl, Kumar, Kishore R., Sue, Carolyn M.

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Newborn Screening for Congenital Adrenal Hyperplasia in India: What Do We Need to Watch Out for? von Kishore Kumar, R., Das, Hari, Kini, Prakash

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Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia von Kumar, Kishore R., Blair, Nicholas F., Vandebona, Himesha, Liang, Christina, Ng, Karl, Sharpe, David M., Grünewald, Anne, Gölnitz, Uta, Saviouk, Viatcheslav, Rolfs, Arndt, Klein, Christine, Sue, Carolyn M.

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Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lange, Lara M., Avenali, Micol, Ellis, Melina, Illarionova, Anastasia, Keller Sarmiento, Ignacio J., Tan, Ai-Huey, Madoev, Harutyun, Galandra, Caterina, Junker, Johanna, Roopnarain, Karisha, Solle, Justin, Wegel, Claire, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore R., Lim, Shen-Yang, Valente, Enza Maria, Nalls, Mike, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, Niccolo, Lohmann, Katja, Klein, Christine

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Ankyloglossia in infancy: An Indian experience von Kishore Kumar, R., Nayana Prabha, P. C., Kumar, Prashant, Patterson, Ruth, Nagar, Nandini

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