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Michael Wangler Lab

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Michael Wangler Lab Publications

Master
Content

2024

  • Gonzalez C, Cohen MJ, Hong J, Calame D, Marri K, Harpavat S, Wangler MF*, Mysore K* (2024). Neuropathy post-liver transplantation in Zellweger Spectrum Disorder: A Case Report. Accepted. Am J Med Genet A
  • Booth KTA, Jangam S, Chui MMC, Treat K, Graziani L, Soldano A, White K, Christensen CK, Lynnes T, Yamamoto S, Kanca O, Tsang MHY, Lynch SA, Mullegama SV, Batista J, Lancu D, Joss SK, Mak CCY, Kwong AY, Bellen HJ, BCM Center for Precision Medicine Models, Conboy E, Sanges R, Wangler MF, Chung BHY, Vetrini F (2024). De novo and inherited variants in DDX39B cause a Novel Syndrome Characterized by Neurodevelopmental Delay, Short Stature, and Congenital Hypotonia.  Accepted Brain. Available on SSRN
  • German RJ, Vuocolo B, Vossaert L, Saba L, The Texome Project, Wangler MF*, Bacino C*, Texome Project (2024). Recurrent carotid paragangliomas in a syndromic patient with a heterozygous missense variant in DNA Methyltransferase 3 Alpha. Am J Med Genet A. Aug 21:e63849 PMID: 39166703
  • Huang Y, Jay KL, Huang A Y-W, Wan J, Jangam SV, Chorin O, Rothschild A, Barel O, Mariani M, Iascone M, Xue H, Undiagnosed Diseases Network, Huang J, Mignot C, Keren B, Saillour V, Mah-Som AY, Sacharow S, Rajabi F, Costin C, Yamamoto S, Kanca, O, Bellen HJ, Rosenfeld JA, Palmer CGS, Nelson SF, Wangler MF*, Marinez-Agosto JA* (2024). Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genet. Med. Jul 19;26(11);101208 PMID: 39036895
  • Vuocolo B, German R, Lalani SR, Murali CN, Bacino CA, Baskin S, Littlejohn R, Odom JD, McLean S, Schmid C, Nutter M, Stuebben M, Magness E, Juarez O, Achi DE, Mitchell B, Glinton KE, Robak L, Nagamani SC, Saba L, Ritenour A, Zhang L, Streff H, Chan K, Kemere KJ, Carter K, The Texome Project*, Owen N, Vossaert L, Liu P, Bellen H, Wangler MF* (2024). Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet. Med. Jun;26(6):101102 PMID: 38431799
     

2023

German RJ, Vuocolo B, Vossaert L, Saba L, The Texome Project, Wangler MF*, Bacino C (2023). Novel Heterozygous Missense Variant in DNMT3A in a Patient with Carotid Paragangliomas (2023). Under review. Am J Med Genet A.

German RJ, Vuocolo B, Vossaert L, Lewis RA, Saba L, The Texome Project, Wangler MF*, Nagamani S (2023). Novel Hemizygous Single Nucleotide Duplication in RPGR in a patient with Retinal Dystrophy and Sensorineural Hearing Loss. In revision. Mol Genet Genomic Med.

Booth KTA, Jangam S, Chui MMC, Treat K, Graziani L, Soldano A, White K, Christensen CK, Lynnes T, Yamamoto S, Kanca O, Tsang MHY, Lynch SA, Mullegama SV, Batista J, Lancu D, Joss SK, Mak CCY, Kwong AY, Bellen HJ, BCM Center for Precision Medicine Models, Conboy E,  Sanges R, Wangler MF, Chung BHY, Vetrini F (2023). .  Submitted. Available on SSRNhttps://doi.org/10.1101/2023.07.15.23292630

Wangler MF, Lesko B, Dahal R, Jangam S, Bhadane P, Wilson TE, McPheron M, Miller MJ(2023). . Mol Genet Metab  140(3):107680. doi: 10.1016/j.ymgme.2023.107680. Online ahead of print. PMID: 37567036

Cara P. Ford, Rebecca O. Littlejohn, Ryan German, Blake Vuocolo, Jose Aceves, Liesbeth Vossaert, Nichole Owen, Wangler MF*, Carrie A (2023). . Mol Genet Genomic Med. e2272. doi: 10.1002/mgg3.2272. Online ahead of print. PMID: 37614148

Yamamoto S, Kanca O, Wangler MF*, Bellen HJ (2023). . Nat Rev Genet. 2023 Jul 25. doi: 10.1038/s41576-023-00633-6. Online ahead of print. PMID: 37491400

Guichard A, Lu S, Kanca O, Bressan D, Huang Y, Ma M, Sanz Juste S, Andrews JC, Jay KL, Sneider M, Schwartz R, Huang MC, Bei D, Pan H, Ma L, Lin WW, Auradkar A, Bhagwat P, Park S, Wan KH, Ohsako T, Takano-Shimizu T, Celniker SE, Wangler MF, Yamamoto S, Bellen HJ, Bier E(2023). . Cell Rep. 42(8):112842. doi: 10.1016/j.celrep.2023.112842. Online ahead of print.  PMID: 37480566.

Jangam S, Briere L, Jay K, Andrews J, Walker M, High F, Yamamoto S, Sweetser D, Wangler MF* (2023). . Genetics. iyad110. doi:10.1093/genetics/iyad110. PMID: 37314226

Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ (2023). . Am J Hum Genet. 110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. PMID: 37054711

Andrews JC, Mok JW, Kanca O, Jangam S, Tifft C, Macnamara EF, Russell BE, Wang LK; Undiagnosed Diseases Network; Nelson SF, Bellen HJ, Yamamoto S, Malicdan MCV, Wangler MF* (2023). . Genet Med. 2023 Mar 31; 100833. doi: 10.1016/j.gim.2023.100833. PMID: 37013900

 

2022

Lyons-Warren AM, Wangler MF, Wan YW (2022).  Int J Mol Sci. 23(21):13030. doi: 10.3390/ijms232113030. PMID: 36361815

Huang Y, Lemire G, Briere LC, Liu F, Wessels MW, Wang X, Osmond M, Kanca O, Lu S, High FA, Walker MA, Rodan LH; Undiagnosed Diseases Network; Care4Rare Canada Consortium, Wangler MF, Yamamoto S, Kernohan KD, Sweetser DA, Boycott KM, Bellen HJ (2022).  Am J Hum Genet. 109(11):2092. doi: 10.1016/j.ajhg.2022.10.001 PMID: 36332614

Lu S, Ma M, Mao X, Bacino CA, Jankovic J, Sutton VR, Bartley JA, Wang X, Rosenfeld JA, Beleza-Meireles A, Chauhan J, Pan X, Li M, Liu P, Prescott K, Amin S, Davies G, Wangler MF, Dai Y, Bellen HJ (2022).  Am J Hum Genet. 109(10):1932-1943. doi: 10.1016/j.ajhg.2022.09.005 PMID: 36206744

Gofin Y, Zhao X, Gerard A, Scaglia F, Wangler MF, Schrier Vergano SA, Scott DA (2022).  Am J Med Genet A. 188(9):2718-2723. doi: 10.1002/ajmg.a.62889. Epub 2022 Jul 7. PMID: 35796094

Grosso BJ, Kramer AA, Tyagi S, Bennett DF, Tifft CJ, D'Souza P, Wangler MF, Macnamara EF, Meza U, Bannister RA (2022). Sci Rep. 12(1):9186. doi: 10.1038/s41598-022-12789-y PMID: 35655070

Barish S, Senturk M, Schoch K, Minogue AL, Lopergolo D, Fallerini C, Harland J, Seemann JH, Stong N, Kranz PG, Kansagra S, Mikati MA, Jasien J, El-Dairi M, Galluzzi P; Undiagnosed Diseases Network, Ariani F, Renieri A, Mari F, Wangler MF, Arur S, Jiang YH, Yamamoto S, Shashi V, Bellen HJ (2022).  Hum Mol Genet. 31(17):2934-2950. doi: 10.1093/hmg/ddac085.  Epub 2022 Apr 1. PMID: 35405010

Thistlethwaite LR, Li X, Burrage LC, Riehle K, Hacia JG, Braverman N, Wangler MF, Miller MJ, Elsea SH, Milosavljevic A (2022).  Sci Rep. 12(1):6556. doi: 10.1038/s41598-022-10415-5. PMID: 35449147

Deisseroth CA, Lerma VC, Magyar CL, Pfliger JM, Nayak A, Bliss ND, LeMaire AW, Narayanan V, Balak C, Zanni G, Valente EM, Bertini E, Benke PJ, Wangler MF, Chao HT (2022).  Ann Neurol. 92(1):138-153. doi: 10.1002/ana.26359. c.  PMID: 35340043.

Marcogliese PC, Deal SL,Andrews J, Harnish JM, Bhavana VH, Graves HK, Jangam S, Luo X, Liu N, Bei D, Chao YH, Hull B, Lee PT, Pan HL, Longley CM, Chao HT, Chung H,  Haelterman NA, Kanca O, Manivannan SN, Rossetti LZ, Gerard A, Schwaibold EMC, Guerrini R, Vetro A,  England E, Murali C, Barakat S,  van Dooren MF, Wilke M, Slegtenhorst MV, Lesca G, Sabatier I, Chatron N, Brownstein CA, Madden JA, Agrawal PB, Keller R, Pavinato L, Brusco A, Rosenfeld JA, Marom R, Wangler MF*, Yamamoto S* (2022).  Cell Rep. 38(11): 110517. doi: 10.1016/j.celrep.2022.110517 PMID: 35294868.

Harnish JM, Li L, Rogic S, Poirier-Morency G, Kim SY; Undiagnosed Diseases Network, Boycott KM, Wangler MF, Bellen HJ, Hieter P, Pavlidis P, Liu Z, Yamamoto S (2022). ModelMatcher:  Hum Mutat. 43(6): 743-759. doi: 10.1002/humu.24364. c. Epub 2022 Feb 27 PMID: 35224820.

Sharma S, Hourigan B, Patel Z, Rosenfeld JA, Chan KM, Wangler MF, Yi JS, Lehman A; CAUSES Study, Horvath G, Cloos PA, Tan Q (2022).  Hum Mutat. 43(7): 889-899. doi: 10.1002/humu.24346. Epub 2022 Feb 14.  PMID: 35165976.