PubRank

C J Curry

Author PubWeight™ 57.64‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Retinoic acid embryopathy. N Engl J Med 1985 5.85
2 Diagnostic criteria for Walker-Warburg syndrome. Am J Med Genet 1989 3.74
3 Tenascin-X deficiency is associated with Ehlers-Danlos syndrome. Nat Genet 1997 2.56
4 Clinical and molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet 1991 2.09
5 The fetal valproate syndrome. Am J Med Genet 1984 2.04
6 A population-based study of congenital diaphragmatic hernia. Teratology 1992 2.04
7 A population-based study of gastroschisis: demographic, pregnancy, and lifestyle risk factors. Teratology 1994 1.84
8 Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome. N Engl J Med 1984 1.70
9 Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality. Am J Med Genet 1987 1.69
10 Familial cases of gastroschisis in a population-based registry. Am J Med Genet 1993 1.57
11 De novo interstitial deletion in the long arm of chromosome 9: a new chromosome syndrome. J Med Genet 1982 1.48
12 Is there an association of Down syndrome and omphalocele? Am J Med Genet 1997 1.44
13 Congenital abnormalities among children with cerebral palsy: More evidence for prenatal antecedents. J Pediatr 2001 1.40
14 Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities. Am J Med Genet 1997 1.38
15 Isolated oral cleft malformations: associations with maternal and infant characteristics in a California population. Teratology 1991 1.17
16 Investigation of nonimmune hydrops fetalis. Am J Obstet Gynecol 1984 1.16
17 Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster. Am J Hum Genet 1999 1.13
18 Maternal medications and environmental exposures as risk factors for gastroschisis. Teratology 1996 1.10
19 Lymphedema in Noonan syndrome: clues to pathogenesis and prenatal diagnosis and review of the literature. Am J Med Genet 1987 1.09
20 The Potter sequence: a clinical analysis of 80 cases. Am J Med Genet 1984 1.08
21 Anorectal and esophageal anomalies with Down syndrome. Am J Med Genet 1992 1.07
22 Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndrome. Clin Genet 1979 1.07
23 Mild autosomal dominant hypophosphatasia: in utero presentation in two families. Am J Med Genet 1999 1.06
24 Rothmund-Thomson syndrome associated with trisomy 8 mosaicism. J Med Genet 1990 1.00
25 Plasma carnitine deficiency. Clinical observations in 51 pediatric patients. Am J Dis Child 1987 0.98
26 Population-based study of tracheoesophageal fistula and esophageal atresia. Teratology 1995 0.98
27 Possible association between the hernia of Morgagni and trisomy 21. Am J Med Genet 1993 0.96
28 Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion. Am J Med Genet 1989 0.94
29 Lethal acantholytic epidermolysis bullosa due to a novel homozygous deletion in DSP: expanding the phenotype and implications for desmoplakin function in skin and heart. Br J Dermatol 2010 0.87
30 Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3. Am J Med Genet 1999 0.87
31 Fellowships and career development in dysmorphology and clinical genetics. Pediatr Clin North Am 1992 0.86
32 Congenital diaphragmatic hernia in the Brachmann-de Lange syndrome. Am J Med Genet 1993 0.86
33 Comments on the Neu-Laxova syndrome and CAD complex. Am J Med Genet 1981 0.86
34 Nucleotide sequence of the p10 polypeptide gene of Autographa californica nuclear polyhedrosis virus. Virology 1984 0.85
35 Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. Am J Med Genet 2000 0.85
36 Nonimmune hydrops fetalis: diagnosis and management. Semin Perinatol 1985 0.83
37 Central nervous system damage and other anomalies in surviving fetus following second trimester antenatal death of co-twin. Report of four cases and literature review. Prenat Diagn 1990 0.83
38 Elucidation of the cytogenetic abnormality in a 4p- "phenocopy". Birth Defects Orig Artic Ser 1982 0.83
39 Prenatal diagnosis of the Beckwith-Wiedemann syndrome. Am J Med Genet 1986 0.81
40 Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome. Birth Defects Orig Artic Ser 1979 0.79
41 D-2-hydroxyglutaric aciduria. J Child Neurol 1995 0.79
42 Ritscher-Schinzel (3C) syndrome: documentation of the phenotype. Am J Med Genet 1997 0.78
43 Neurofibromatosis-Noonan syndrome. Pediatr Dermatol 1995 0.77
44 Cerebrovascular disorders in children with the factor V Leiden mutation. J Child Neurol 2001 0.76
45 Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child. Am J Med Genet 2000 0.75
46 Lower limb deficiency and the urethral obstruction sequence. Birth Defects Orig Artic Ser 1982 0.75
47 Further comments on the Neu-Laxova syndrome. Am J Med Genet 1982 0.75
48 Pigment analysis in the forensic examination of paints. I. Pigment analysis by X-ray powder diffraction. J Forensic Sci Soc 1982 0.75
49 New mesomelic dysplasia with absent fibulae and triangular tibiae. Am J Med Genet 2000 0.75
50 Hodgkin's disease complicating neuronal ceroid-lipofuscinosis. Am J Pediatr Hematol Oncol 1989 0.75
51 False negative results in patients with fra(X) (q) mental retardation taking oral vitamin supplements. N Engl J Med 1987 0.75