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Impact of integrated translational research on clinical exome sequencing.
Genet Med. 2021 Mar;23(3):498-507. doi: 10.1038/s41436-020-01005-9. Epub 2020 Nov 4.
Genet Med. 2021.
PMID: 33144682
Free article.
Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome.
Samadder NJ, Riegert-Johnson D, Boardman L, Rhodes D, Wick M, Okuno S, Kunze KL, Golafshar M, Uson PLS Jr, Mountjoy L, Ertz-Archambault N, Patel N, Rodriguez EA, Lizaola-Mayo B, Lehrer M, Thorpe CS, Yu NY, Esplin ED, Nussbaum RL, Sharp RR, Azevedo C, Klint M, Hager M, Macklin-Mantia S, Bryce AH, Bekaii-Saab TS, Sekulic A, Stewart AK.
Samadder NJ, et al.
JAMA Oncol. 2021 Feb 1;7(2):230-237. doi: 10.1001/jamaoncol.2020.6252.
JAMA Oncol. 2021.
PMID: 33126242
Free PMC article.
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Recurrent ganglioneuroma in PTPN11-associated Noonan syndrome: A case report and literature review.
Morales-Rosado JA, Singh H, Olson RJ, Larsen BT, Hager MM, Klee EW, Dhamija R.
Morales-Rosado JA, et al. Among authors: hager mm.
Am J Med Genet A. 2021 Jun;185(6):1883-1887. doi: 10.1002/ajmg.a.62178. Epub 2021 Mar 29.
Am J Med Genet A. 2021.
PMID: 33779033
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Genomics Integration Into Nephrology Practice.
Pinto E Vairo F, Prochnow C, Kemppainen JL, Lisi EC, Steyermark JM, Kruisselbrink TM, Pichurin PN, Dhamija R, Hager MM, Albadri S, Cornell LD, Lazaridis KN, Klee EW, Senum SR, El Ters M, Amer H, Baudhuin LM, Moyer AM, Keddis MT, Zand L, Sas DJ, Erickson SB, Fervenza FC, Lieske JC, Harris PC, Hogan MC.
Pinto E Vairo F, et al. Among authors: hager mm.
Kidney Med. 2021 Jun 29;3(5):785-798. doi: 10.1016/j.xkme.2021.04.014. eCollection 2021 Sep-Oct.
Kidney Med. 2021.
PMID: 34746741
Free PMC article.
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Impact of integrated translational research on clinical exome sequencing.
Klee EW, Cousin MA, Pinto E Vairo F, Morales-Rosado JA, Macke EL, Jenkinson WG, Ferrer A, Schultz-Rogers LE, Olson RJ, Oliver GR, Sigafoos AN, Schwab TL, Zimmermann MT, Urrutia RA, Kaiwar C, Gupta A, Blackburn PR, Boczek NJ, Prochnow CA, Lowy RJ, Mulvihill LA, McAllister TM, Aoudia SL, Kruisselbrink TM, Gunderson LB, Kemppainen JL, Fisher LJ, Tarnowski JM, Hager MM, Kroc SA, Bertsch NL, Agre KE, Jackson JL, Macklin-Mantia SK, Murphree MI, Rust LM, Summer Bolster JM, Beck SA, Atwal PS, Ellingson MS, Barnett SS, Rasmussen KJ, Lahner CA, Niu Z, Hasadsri L, Ferber MJ, Marcou CA, Clark KJ, Pichurin PN, Deyle DR, Morava-Kozicz E, Gavrilova RH, Dhamija R, Wierenga KJ, Lanpher BC, Babovic-Vuksanovic D, Farrugia G, Schimmenti LA, Stewart AK, Lazaridis KN.
Klee EW, et al. Among authors: hager mm.
Genet Med. 2023 Feb;25(2):100359. doi: 10.1016/j.gim.2022.12.006.
Genet Med. 2023.
PMID: 36745126
Free article.
No abstract available.
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COL4A4 variant recently identified: lessons learned in variant interpretation-a case report.
Cocorpus J, Hager MM, Benchimol C, Bijol V, Salem F, Punj S, Castellanos L, Singer P, Sethna CB, Basalely A.
Cocorpus J, et al. Among authors: hager mm.
BMC Nephrol. 2022 Jul 16;23(1):253. doi: 10.1186/s12882-022-02866-9.
BMC Nephrol. 2022.
PMID: 35842573
Free PMC article.
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