COVCOG 2: Cognitive and Memory Deficits in Long COVID: A Second Publication From the COVID and Cognition Study von Guo, Panyuan, Benito Ballesteros, Alvaro, Yeung, Sabine P, Liu, Ruby, Saha, Arka, Curtis, Lyn, Kaser, Muzaffer, Haggard, Mark P, Cheke, Lucy G

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COVCOG 1: Factors Predicting Physical, Neurological and Cognitive Symptoms in Long COVID in a Community Sample. A First Publication From the COVID and Cognition Study von Guo, Panyuan, Benito Ballesteros, Alvaro, Yeung, Sabine P, Liu, Ruby, Saha, Arka, Curtis, Lyn, Kaser, Muzaffer, Haggard, Mark P, Cheke, Lucy G

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P696: Case presentation: Co-segregation of a rare GLA variant of uncertain significance within 2 multiplex families facilitates variant reclassification to pathogenic von Colasanto, Mary, Pan, Yinghong, Liu, Ruby, Collins, Christin, Hegde, Madhuri

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P599: Beyond single nucleotide variants and copy number variations: Spinal muscular atrophy and repeat expansion disorders screening by whole genome sequencing von Liu, Ruby, Reddy Nallamilli, Babi Ramesh, Collins, Christin, Bean, Lora, Hegde, Madhuri

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P729: Identification of multiple diagnoses in pediatric patients through genome sequencing von Collins, Christin, Guo, Fen, Liu, Ruby, Pan, Yinghong, Colasanto, Mary, Hegde, Madhuri

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P519: Evidence of complex inheritance patterns in limb-girdle and other muscular dystrophies: Synergistic heterozygosity and multigenic inheritance von Hegde, Madhuri, Nallamilli, Babi, Pan, Yinghong, Lakshmanan, Jagannathan, Ramachander, Vinish, Liu, Ruby

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P476: Identification and accurate sizing of D4Z4 repeat units in patients suspected of facioscapulohumeral muscular dystrophy (FSHD) using optical genome mapping von Guruju, Naga, Jump, Vanessa, Nallamilli, Babi, Liu, Ruby, Luo, Zhiwen, Hegde, Madhuri

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P638: Genomic breakpoint analysis facilitates identification of complex rearrangements and re-classification of non-tandem duplications in the DMD gene von Guruju, Naga, Jump, Vanessa, Liu, Ruby, Reddy Nallamilli, Babi Ramesh, Steigerwalt, Jill, Collins, Christin, Bean, Lora, Hegde, Madhuri

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P643: Unveiling noncoding DMD variants: Synergizing RNA sequencing and DNA sequencing for enhanced molecular diagnosis von Pan, Yinghong, Guo, Fen, Ma, Zeqiang, Reddy Nallamilli, Babi Ramesh, Liu, Ruby, Quirin, Kayla, Martin, Ann, Hegde, Madhuri

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P502: How does multiomics help variant reclassification? von Liu, Ruby, Guo, Fen, Reddy Nallamilli, Babi Ramesh, Collins, Christin, Bean, Lora, Guruju, Naga, Hegde, Madhuri

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P639: Prenatal diagnosis of Alkuraya-Kučinskas syndrome by exome sequencing von Rice, Stephanie, Varotsis, Dante, Wodoslawsky, Sascha, Critchlow, Elizabeth, Liu, Ruby, Berger, Seth, Al-Kouatly, Huda

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P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders von Nallamilli, Babi Ramesh Reddy, Lakshmanan, Jagannathan, Ramachander, Vinish, Dhillon, Supan, Liu, Ruby, Pan, Yinghong, Guruju, Naga, Collins, Christin, Bean, Lora, Hegde, Madhuri

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P714: Genome screening of newborns: Sequencing is easy, assessing the clinical utility of genomic findings uncovered in asymptomatic children is challenging von Balciuniene, Jorune, Liu, Ruby, Bean, Lora, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Fura, Kristina, Chin, Eprem, Mathur, Abhinav, Ma, Zeqiang, Carmichael, Jonathan, Collins, Christin, da Silva, Cristina, Kirmse, Brian, Bleyl, Steven, Hegde, Madhuri

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P425: Unparalleled power of genome sequencing in screening ostensibly healthy newborns and children: Findings from the first real-world dataset von Balciuniene, Jorune, Liu, Ruby, Collins, Christin, Bean, Lora, Guo, Fen, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Fura, Kristina, Chin, Ephrem, da Silva, Cristina, Mathur, Abhinav, Ma, Zeqiang, Hegde, Madhuri

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P389: Real-world evidence demonstrating why genome sequencing should be recommended as the first-tier genetic test von Guo, Fen, Liu, Ruby, Pan, Yinghong, Collins, Christin D., Bean, Lora, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Chin, Ephrem, da Silva, Cristina, Mathur, Abhinav, Ma, Zeqiang, Balciuniene, Jorune, Hegde, Madhuri

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P426: Recognizing the promise and potential pitfalls of genomic medicine through routine rapid whole genome sequencing von Bean, Lora, Collins, Christin, Guo, Fen, Balciuniene, Jorune, Chen-Deutsch, Xiangwen, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Yousaf, Rizwan, Fura, Kristina, Woodman, Amber, Liu, Ruby, Zhang, Jenny, Liebmann, Kate, Gerow, Julia, Chin, Ephrem, Hegde, Madhuri

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Polyethylene terephthalate nanoparticles induce oxidative damage in Chlorella vulgaris von Vijayan, Siji, Liu, Ruby, George, Saji, Bhaskaran, Sinilal

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Beyond Single Diagnosis: Exploring Multidiagnostic Realities in Pediatric Patients through Genome Sequencing von Guo, Fen, Liu, Ruby, Pan, Yinghong, Colasanto, Mary, Collins, Christin, Hegde, Madhuri

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Influencing human–AI interaction by priming beliefs about AI can increase perceived trustworthiness, empathy and effectiveness von Pataranutaporn, Pat, Liu, Ruby, Finn, Ed, Maes, Pattie

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eP370 - Fascioscapulohumeral muscular dystrophy genetic testing by optic mapping von Hegde, Madhuri, Behlmann, Andrea, Shenoy, Suresh, Liu, Ruby

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