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Longoni M, Russell MK, High FA, Darvishi K, Maalouf FI, Kashani A, Tracy AA, Coletti CM, Loscertales M, Lage K, Ackerman KG, Woods SA, Ward-Melver C, Andrews D, Lee C, Pober BR, Donahoe PK. "Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia." Clinical genetics. 2015 Apr; 87(4):362-7. Epub 2014 Apr 26.


Longoni M, High FA, Russell MK, Kashani A, Tracy AA, Coletti CM, Hila R, Shamia A, Wells J, Ackerman KG, Wilson JM, Bult CJ, Lee C, Lage K, Pober BR, Donahoe PK. "Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics." Proceedings of the National Academy of Sciences of the United States of America. 2014 Aug 26; 111(34):12450-5. Epub 2014 Aug 08.


Coles GL, Ackerman KG. "Kif7 is required for the patterning and differentiation of the diaphragm in a model of syndromic congenital diaphragmatic hernia." Proceedings of the National Academy of Sciences of the United States of America. 2013 May 21; 110(21):E1898-905. Epub 2013 May 06.

Hall MW, Geyer SM, Guo CY, Panoskaltsis-Mortari A, Jouvet P, Ferdinands J, Shay DK, Nateri J, Greathouse K, Sullivan R, Tran T, Keisling S, Randolph AG, . "Innate immune function and mortality in critically ill children with influenza: a multicenter study." Critical care medicine. 2013 Jan; 41(1):224-36.


Russell MK, Longoni M, Wells J, Maalouf FI, Tracy AA, Loscertales M, Ackerman KG, Pober BR, Lage K, Bult CJ, Donahoe PK. "Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes." Proceedings of the National Academy of Sciences of the United States of America. 2012 Feb 21; 109(8):2978-83. Epub 2012 Feb 06.

Ackerman KG; Vargas SO; Wilson JM; Jennings RW; Kozakewich HP; Pober B. "Congenital Diaphragmatic Defects: Proposal for a New Classification Based on Observations in 234 Patients." Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 2012; Epub 2012 Mar 07.


Kantarci S, Ackerman KG, (co-first authors Russell M, Longoni M, Sougnez C, Noonan KM, Hatchwell E, Zhang X, Canmarcke, RP,Anyane-Yeboe K, Dickman P, Wilson J, Donahue P, Pober BR). "Characterization of the Chromosome 1q41q42.12 region and the Candidate Gene DISP1, in Patients with CDH". American Journal of Medical Genetics. 2010; .


Liu, X.; Ramjiganesh, T.; Chen, Y.H.; Chung, S.W.; Hall, S.R.; Schissel, S.L.; Padera, R.F. Jr.; Liao, R.; Ackerman, K.G.; Kajstura, J.; Leri, A.; Anversa, P.; Yet, S.F.; Layne, M.D.; Perrella M.A. "Disruption of striated preferentially expressed gene locus leads to dilated cardiomyopathy in mice." Circulation. 2009; 119(2): 261-268.

Zhou, B; Ma, Q; Kong, SW; Hu, Y; Campbell, PH; McGowan, FX; Ackerman, KG; Wu, B; Zhou, B; Tevosian, SG; Pu, WT. "Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart". J Clin Invest. 2009; 119(6): 1462-1476.

Stevens TP; van Wijngaarden E; Ackerman KG; Lally PA; Lally KP; . "Timing of delivery and survival rates for infants with prenatal diagnoses of congenital diaphragmatic hernia." Pediatrics. 2009; 123(2):494-502.


Ackerman KG; Wang J; Luo L; Fujiwara Y; Orkin SH; Beier DR. "Gata4 is necessary for normal pulmonary lobar development." American journal of respiratory cell and molecular biology. 2007; 36(4):391-7. Epub 2006 Dec 01.

Pober, B.R.; Lin, A.; Russell, M.; Ackerman, K.G.; Chakravorty, S.; Strauss, B.; Westgate, M. N.; Wilson, J.; Donahoe, P.K.; Holmes, L.B. "Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program." Am.J.Med.Genet.A.. 2005; 138(2): 81-88.


Ackerman KG; Huang H; Grasemann H; Puma C; Singer JB; Hill AE; Lander E; Nadeau JH; Churchill GA; Drazen JM; Beier DR. "Interacting genetic loci cause airway hyperresponsiveness." Physiological genomics. 2005; 21(1):105-11. Epub 2005 Jan 18.

Ackerman KG; Herron BJ; Vargas SO; Huang H; Tevosian SG; Kochilas L; Rao C; Pober BR; Babiuk RP; Epstein JA; Greer JJ; Beier DR. "Fog2 is required for normal diaphragm and lung development in mice and humans." PLoS genetics. 2005; 1(1):58-65. Epub 2005 Jun 17.


Levy, BD; De Sanctis, GT; Devchand, PR; Kim, E; Ackerman, K; Schmidt, B; Szczeklik, W; Drazen, JM; Serhan, CN. "Lipoxins and aspirin-triggered lipoxins in airway responses". Adv Exp Med Biol. 2003; 525: 19-23.


Levy, BD; De Sanctis, GT; Devchand, PR; Kim, E; Ackerman, K; Schmidt, BA; Szczeklik, W; Drazen, JM; Serhan, CN. "Multi-pronged inhibition of airway hyper-responsiveness and inflammation by lipoxin A(4)". Nat Med. 2002; 8(9): 1018-1023.

Finotto, S; Neurath, MF; Glickman, JN; Qin, S; Lehr, HA; Green, FH; Ackerman, K; Haley, K; Galle, PR; Szabo, SJ; Drazen, JM; De Sanctis, GT; Glimcher, LH. "Development of spontaneous airway changes consistent with human asthma in mice lacking T-bet". Science. 2002; 295(5553): 336-338.


Grover, T.R.; Ackerman, K.G.; Le Cras, T.D.; Jobe, A.H.; Abman, S.H. "Repetitive prenatal glucocorticoids increase lung endothelial nitric oxide synthase expression in ovine fetuses delivered at term." Pediatric Res.. 2000; 48(1): 75-83.

MacLean, JA; De Sanctis, GT; Ackerman, KG; Drazen, JM; Sauty, A; DeHaan, E; Green, FH; Charo, IF; Luster, AD. "CC chemokine receptor-2 is not essential for the development of antigen-induced pulmonary eosinophilia and airway hyperresponsiveness". J Immunology. 2000; 165(11): 6568-6575.

Rogers, B; Msall, M; Owens, T; Guernsey, K; Brody, A; Buck, G; Hudak, M. "Cystic periventricular leukomalacia and type of cerebral palsy in preterm infants". J Pediatr. 1994; 125(1): S1-S8.