Human
Human cytomegalovirus in breast milk is associated with milk composition and the infant gut microbiome and growth (2024)
Kelsey E. Johnson, Nelmary Hernandez-Alvarado, Mark Blackstad, Timothy Heisel, Mattea Allert, David A. Fields, Elvira Isganaitis, Katherine M. Jacobs, Dan Knights, Eric F. Lock, Michael C. Rudolph, Cheryl A. Gale, Mark R. Schleiss, Frank W. Albert, Ellen W. Demerath & Ran Blekhman
Human
Cell-type-specific and disease-associated expression quantitative trait loci in the human lung (2024)
Heini M Natri, Christina B Del Azodi, Lance Peter, Chase J Taylor, Sagrika Chugh, Robert Kendle, Mei-i Chung, David K Flaherty, Brittany K Matlock, Carla L Calvi, Timothy S Blackwell, Lorraine B Ware, Matthew Bacchetta, Rajat Walia, Ciara M Shaver, View ORCID ProfileJonathan A Kropski, View ORCID ProfileDavis J McCarthy, Nicholas E Banovich
Human
Interleukin-1 receptor antagonist gene (IL1RN) variants modulate the cytokine release syndrome and mortality of COVID-19 (2024)
Mukundan Attur, Christopher Petrilli, Samrachana Adhikari, Eduardo Iturrate, Xiyue Li, Stephanie Tuminello, Nan Hu, Aravinda Chakravarti, David Beck, Steven B Abramson
Human
A comparison between low-cost library preparation kits for low coverage sequencing (2024)
Caitlin M. Stewart, Matthew JS Gibson, Jahan-Yar Parsa, Jeremiah H. Li
Human
Concordance of whole-genome amplified embryonic DNA with the subsequently born child (2024)
Shenglai Li, Thomas Giardina, Maria Katz, Dhruva Chandramohan, Nathan Slotnick, Barry Behr, Noor Siddiqui, Yuntao Xia, Benjamin Podgursky
Human
First clinical validation of whole genome screening on standard trophectoderm biopsies of preimplantation embryos (2024)
Yuntao Xia, Maria Katz, Dhruva Chandramohan, Elan Bechor, Ben Podgursky, Michael Hoxie, Qinnan Zhang, Willy Chertman, Jessica Kang, Edwina Blue, Justin Chen, Justin Schleede, Nathan R. Slotnick, Xiaoli Du, Robert Boostanfar, Eric Urcia, Barry Behr, Jacques Cohen, Noor Siddiqui
Human
GWAS and PRS-PheWAS across complex phenotypes in the human phenotype project (2024)
Zachary Levine, Iris Kalka, Dmitry Kolobkov, Hagai Rossman, Anastasia Godneva, Smadar Shilo, Ayya Keshet, Daphna Weissglas-Volkov, Tal Shor, Alon Diament, Yeela Talmor-Barkan, Yaron Aviv, Tom Sharon, Adina Weinberger, Eran Segal
Human
Low-pass sequencing plus imputation using avidity sequencing displays comparable imputation accuracy to sequencing by synthesis while reducing duplicates (2024)
Jeremiah H Li, Karrah Findley, Joseph K Pickrell, Kelly Blease, Junhua Zhao, Semyon Kruglyak
Human
Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations (2023)
Boris Noyvert, A Mesut Erzurumluoglu, Dmitriy Drichel, Steffen Omland, Till F M Andlauer, Stefanie Mueller, Lau Sennels, Christian Becker, Aleksandr Kantorovich, Boris A Bartholdy, Ingrid Brænne, Julio Cesar Bolivar-Lopez, Costas Mistrellides, Gillian M Belbin, Jeremiah H Li, Joseph K Pickrell, Johann de Jong, Jatin Arora, Yao Hu, Boehringer Ingelheim – Global Computational Biology and Digital Sciences, Clive R Wood, Jan M Kriegl, Nikhil Podduturi, Jan N Jensen, Jan Stutzki, Zhihao Ding
Human
Evaluation of noninvasive biospecimens for transcriptome studies (2023)
Molly Martorella, Silva Kasela, Renee Garcia-Flores, Alper Gokden, Stephane E. Castel & Tuuli Lappalainen
Human
The effects of reference panel perturbations on the accuracy of genotype imputation (2023)
Jeremiah H. Li, Andrew Liu, C. Alex Buerkle, William Palmer, Gillian M. Belbin, Mohammad Ahangari, Matthew J.S. Gibson, Lex Flagel
Human