New ideas in epilepsy genetics : Novel epilepsy genes, copy number alterations, and gene regulationGURNETT, Christina A; HEDERA, Peter.Archives of neurology (Chicago). 2007, Vol 64, Num 3, pp 324-328, issn 0003-9942, 5 p.Article

Analysis of cerebrospinal fluid glial fibrillary acidic protein after seizures in childrenGURNETT, Christina A; LANDT, Michael; WONG, Michael et al.Epilepsia (Copenhagen). 2003, Vol 44, Num 11, pp 1455-1458, issn 0013-9580, 4 p.Article

Update on Clubfoot : Etiology and Treatment : Clubfoot: etiology and treatmentDOBBS, Matthew B; GURNETT, Christina A.Clinical orthopaedics and related research. 2009, Vol 467, Num 5, pp 1146-1153, issn 0009-921X, 8 p.Article

Magnetic Resonance Angiography in Clubfoot and Vertical Talus : A Feasibility Study : Clubfoot: etiology and treatmentKRUSE, Lisa; GURNETT, Christina A; HOOTNICK, David et al.Clinical orthopaedics and related research. 2009, Vol 467, Num 5, pp 1250-1255, issn 0009-921X, 6 p.Article

Vascular Abnormalities Correlate with Decreased Soft Tissue Volumes in Idiopathic ClubfootMERRILL, Laura J; GURNETT, Christina A; SIEGEL, Marilyn et al.Clinical orthopaedics and related research. 2011, Vol 469, Num 5, pp 1442-1449, issn 0009-921X, 8 p.Article

Skeletal Muscle Abnormalities and Genetic Factors Related to Vertical TalusMERRILL, Laura J; GURNETT, Christina A; CONNOLLY, Anne M et al.Clinical orthopaedics and related research. 2011, Vol 469, Num 4, pp 1167-1174, issn 0009-921X, 8 p.Article

Disruption of Sodium Bicarbonate Transporter SLC4A10 in a Patient With Complex Partial Epilepsy and Mental RetardationGURNETT, Christina A; VEILE, Rose; ZEMPEL, John et al.Archives of neurology (Chicago). 2008, Vol 65, Num 4, pp 550-553, issn 0003-9942, 4 p.Article

Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus : Genetics in OrthopaedicsGURNETT, Christina A; KEPPEL, Cassie; BICK, Jennifer et al.Clinical orthopaedics and related research. 2007, Num 462, pp 27-31, issn 0009-921X, 5 p.Article

Exome Sequencing Identifies an MYH3 Mutation in a Family with Distal Arthrogryposis Type 1ALVARADO, David M; BUCHAN, Jillian G; GURNETT, Christina A et al.Journal of bone and joint surgery. American volume (Print ed.). 2011, Vol 93A, Num 11, pp 1045-1050, issn 0021-9355, 6 p.Article

Skeletal Muscle Contractile Gene (TNNT3, MYH3, TPM2) Mutations Not Found in Vertical Talus or Clubfoot : Clubfoot: etiology and treatmentGURNETT, Christina A; ALAEE, Farhang; DESRUISSEAU, David et al.Clinical orthopaedics and related research. 2009, Vol 467, Num 5, pp 1195-1200, issn 0009-921X, 6 p.Article

Congenital Knee Dislocation in a Patient with Larsen Syndrome and a Novel Filamin B MutationDOBBS, Matthew B; BOEHM, Stephanie; GRANGE, Dorothy K et al.Clinical orthopaedics and related research. 2008, Vol 466, Num 6, pp 1503-1509, issn 0009-921X, 7 p.Article

Flexor digitorum accessorius longus muscle is associated with familial idiopathic clubfootDOBBS, Matthew B; WALTON, Tim; GORDON, J. Eric et al.Journal of pediatric orthopedics. 2005, Vol 25, Num 3, pp 357-359, issn 0271-6798, 3 p.Article

Factors predictive of outcome after use of the ponseti method for the treatment of idiopathic clubfeetDOBBS, Matthew B; RUDZKI, J. R; PURCELL, Derek B et al.Journal of bone and joint surgery. American volume. 2004, Vol 86A, Num 1, pp 22-27, issn 0021-9355, 6 p.Article

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1GURNETT, Christina A; DESRUISSEAU, David M; DRULEY, Todd E et al.Human molecular genetics (Print). 2010, Vol 19, Num 7, pp 1165-1173, issn 0964-6906, 9 p.Article

Early Results of the Ponseti Method for the Treatment of Clubfoot Associated with MyelomeningoceleGERLACH, David J; GURNETT, Christina A; LIMPAPHAYOM, Noppachart et al.Journal of bone and joint surgery. American volume (Print ed.). 2009, Vol 91A, Num 6, pp 1350-1359, issn 0021-9355, 10 p.Article

Variants in Genes That Encode Muscle Contractile Proteins Influence Risk for Isolated ClubfootWEYMOUTH, Katelyn S; BLANTON, Susan H; HECHT, Jacqueline T et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 9, pp 2170-2179, issn 1552-4825, 10 p.Article

DICER1 Mutations in Familial Pleuropulmonary BlastomaASHLEY HILL, D; IVANOVICH, Jennifer; WILLIAM, Gretchen et al.Science (Washington, D.C.). 2009, Vol 325, Num 5943, issn 0036-8075, p. 965Article

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genesSHARMA, Swarkar; XIAOCHONG GAO; GURNETT, Christina A et al.Human molecular genetics (Print). 2011, Vol 20, Num 7, pp 1456-1466, issn 0964-6906, 11 p.Article

Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in miceALVARADO, David M; MCCALL, Kevin; AFEROL, Hyuliya et al.Human molecular genetics (Print). 2011, Vol 20, Num 20, pp 3943-3952, issn 0964-6906, 10 p.Article

Familial Isolated Clubfoot Is Associated with Recurrent Chromosome 17q23.1q23.2 Microduplications Containing TBX4ALVARADO, David M; AFROL, Hyuliya; MCCALL, Kevin et al.American journal of human genetics. 2010, Vol 87, Num 1, pp 154-160, issn 0002-9297, 7 p.Article

Altered Transmission of HOX and Apoptotic SNPs Identify a Potential Common Pathway for ClubfootESTER, Audrey R; WEYMOUTH, Katelyn S; BURT, Amber et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 12, pp 2745-2752, issn 1552-4825, 8 p.Article

Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3GURNETT, Christina A; DOBBS, Matthew B; NORDSIECK, Eric J et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 16, pp 1744-1748, issn 1552-4825, 5 p.Article