Krall, M. "Racial Disparities Between Black and White Patients in Joint Replacement Surgery: A Systematic Review" , American College of Rheumatology Meeting, San Diego, CA: 2023
Krall, M. "A 46 Year Old man With a History of Autoimmune Myositis Presents With Fatigue and Fever" , 39th Carl M Pearson Memorial Symposium: Frontiers of Rheumatology Conference, Marina del Rey, California: 2021
Islam F, Htun S, Lai LW, Krall M, Poranki M, Martin PM, Sobreira N, Wohler ES, Yu J, Moore AT, Slavotinek AM "Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population" , Clin Genet, 98(5): 2020,499-506
Krall M, Htun S, Schnur RE "Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies." , Eur. J. Hum. Genet, 27(4): 2019,582-93
Krall M, Htun S, Slavotinek A "Use of PTC124 for nonsense suppression therapy targeting BMP4 nonsense variants in vitro and the bmp4st72 allele in zebrafish" , PLoS One, 14(4): 2019
Zhong Ye, Chun Wang, Shaogui Wan, Zhaomei Mu, Zhenchao Zhang, Maysa M Abu-Khalaf, Frederick M Fellin, Daniel P Silver, Manish Neupane, Rebecca J Jaslow, Saveri Bhattacharya, Theodore N Tsangaris, Inna Chervoneva, Adam Berger, Laura Austin, Juan P Palazzo, Ronald E Myers, Neha Pancholy, Darayus Toorkey, Kaelan Yao, Max Krall, Xiuling Li, Xiaobing Chen, Xiuhong Fu, Jinliang Xing, Lifang Hou 11, Qiang Wei, Bingshan Li, Massimo Cristofanilli, Hushan Yang "Association of clinical outcomes in metastatic breast cancer patients with circulating tumour cell and circulating cell-free DNA " , Eur J Cancer: 2019,133-43
Krall M, Htun S, Anand D "A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans" , Hum. Genet, 137(5): 2018,427-8
Kievit A, Tessadori F, Douben H, Krall M "Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome" , Eur. J. Hum. Genet, 26(2): 2018,210-9
Bardakjian T, Krall M Wu D "A recurrent, non-penetrant sequence variant, p.Arg266Cys in Growth/Differentiation Factor 3 (GDF3) in a female with unilateral anophthalmia and skeletal anomalies" , Am. J. Ophthalmol, 21(7): 2017,102-6
Krall, M., Slavotinek, A. "Microphthalmia and Anterior Segment Abnormalities in a Zebrafish Model of foxe3 Loss of Function Using CRISPR/Cas9" , ACMG Annual Clinical Genetics Meeting in Phoenix, Arizona: 2017
