PubRank

A D Merritt

Author PubWeight™ 55.49‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Linkage group I: the simultaneous estimation of recombination and interference. Birth Defects Orig Artic Ser 1976 8.63
2 Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies. Am J Hum Genet 1973 3.12
3 Osteopetrosis. A clinical, genetic, metabolic, and morphologic study of the dominantly inherited, benign form. Medicine (Baltimore) 1968 2.39
4 Hepatitis A outbreaks among illicit drug users and their contacts in Queensland, 1997. Med J Aust 1999 2.05
5 Differential expression of salivary (Amy1) and pancreatic (Amy2) human amylase loci in prenatal and postnatal development. J Med Genet 1976 1.42
6 Holoprosencephaly: birth data, benetic and demographic analyses of 30 families. Birth Defects Orig Artic Ser 1975 1.40
7 Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. Am J Hum Genet 1973 1.38
8 Hyperamylasemia in diabetic ketoacidosis: sources and significance. Ann Intern Med 1979 1.36
9 Human salivary amylase: genetics of electrophoretic variants. Am J Hum Genet 1971 1.33
10 Evidence for close linkage of human amylase loci. Nat New Biol 1972 1.32
11 Ring chromosome 18 in a patient with multiple anomalies. J Med Genet 1967 1.30
12 Simplified method for collection of pure submandibular saliva in large volumes. J Dent Res 1968 1.28
13 Two contiguous outbreaks of dengue type 2 in north Queensland. Med J Aust 1998 1.26
14 Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus. Am J Hum Genet 1977 1.23
15 The hepatitis knowledge base (short form). Ann Intern Med 1980 1.22
16 Genetic family history questionnaire. J Med Genet 1978 1.21
17 A syndrome of bizarre vertebral anomalies. J Pediatr 1966 1.10
18 Evidence for post-transcriptional modification of human salivary amylase (amyl) isozymes. Biochem Genet 1973 1.06
19 Genetic control of the eighth component of complement. J Clin Invest 1979 1.03
20 Immunological relationships and post-translational modification of human salivary amylase (Amy) and pancreatic amylase (Amy) isozymes. Biochem Genet 1974 1.03
21 Familial myocardial disease with and without obstruction to left ventricular outflow. Clinical, hemodynamic, and angiographic findings. Circulation 1967 1.03
22 Cystic fibrosis: population genetics. Tex Rep Biol Med 1973 1.02
23 Linkage relationships and multipoint mapping of the human parotid salivary proteins (Pr, Pa, Db). Am J Hum Genet 1980 1.00
24 Linkage group I: a statistically significant locus order from family studies. Cytogenet Cell Genet 1978 0.99
25 Partial purification and characterization of a polymorphic protein (Pa) in human parotid saliva. Am J Hum Genet 1975 0.99
26 Genetic studies of human acidic salivary protein (Pa). Am J Hum Genet 1975 0.97
27 Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studies. Cytogenet Cell Genet 1978 0.93
28 Autosomal dominant "spheroid body myopathy". Muscle Nerve 1979 0.91
29 Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. Birth Defects Orig Artic Ser 1975 0.88
30 Urinary pepsinogen isozymes: a highly polymorphic locus in man. Hum Genet 1979 0.85
31 The tissue origins of serum and urinary alpha-amylase. Arch Biochem Biophys 1976 0.84
32 Linkage group I: the simultaneous estimation of recombination and interference. Cytogenet Cell Genet 1976 0.84
33 Linkage relationships of the proline-rich salivary proteins (Pr, Pa, Db). Cytogenet Cell Genet 1978 0.83
34 Human salivary proline-rich (Pr) proteins: a posttranslational derivation of the phenotypes. Biochem Genet 1979 0.81
35 Heritable salivary proteins and dental disease. Hum Hered 1980 0.80
36 Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA). Cytogenet Cell Genet 1976 0.80
37 Genetic linkage studies in Huntington disease. Cytogenet Cell Genet 1978 0.79
38 Genetic analysis of urinary pepsinogen isozymes. Cytogenet Cell Genet 1978 0.79
39 The linkage and mapping relationships of 1 qh. Cytogenet Cell Genet 1976 0.78
40 Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA). Birth Defects Orig Artic Ser 1976 0.78
41 The human alpha-amylases. Adv Hum Genet 1977 0.78
42 Genetic studies of tooth size factors in Pima Indian families. Am J Hum Genet 1968 0.75
43 Human pancreatic alpha-amylase: phenotypic codominance and new electrophoretic variants. Am J Hum Genet 1978 0.75
44 The utilization of a written family history questionnaire in genetic counseling. Birth Defects Orig Artic Ser 1978 0.75
45 Do brine shrimp diagnose cystic fibrosis? Pediatr Res 1975 0.75
46 Genetic counseling at the Indiana University Medical Center. J Indiana State Med Assoc 1974 0.75
47 Community needs, availability of resources and education. Birth Defects Orig Artic Ser 1970 0.75
48 Linkage group I: multipoint mapping. Cytogenet Cell Genet 1975 0.75
49 Electrophoretic analysis of serum proteins in cystic fibrosis. Pediatr Res 1977 0.75
50 Genetic variants of thyroxine-binding globulin (TBG). Birth Defects Orig Artic Ser 1971 0.75
51 Immunohistochemical demonstration of the loss of immunoreactive amylase from neoplastic human salivary gland. Experientia 1981 0.75
52 A perspective from the Knowledge Base Research Program (KBRP). J Clin Comput 1983 0.75
53 Electrophoretic analysis of serum proteins in cystic fibrosis. Pediatr Res 1977 0.75
54 Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. Cytogenet Cell Genet 1975 0.75
55 An amylase-producing serous cystadenocarcinoma of the ovary. Oncology 1985 0.75
56 Dominantly inherited periodic bone pain. Birth Defects Orig Artic Ser 1974 0.75
57 Linkage group I: multipoint mapping. Birth Defects Orig Artic Ser 1975 0.75
58 Immunological and chemical comparison on heterogeneous basic glycoproteins in human parotid saliva. Biochim Biophys Acta 1971 0.75
59 A system for the retrieval of family structured information. Comput Biol Med 1977 0.75
60 Leukocyte abnormalities in familial amaurotic idiocy. N Engl J Med 1966 0.75
61 An evaluation of differential methylation of ribonucleic acid in cystic fibrosis. Pediatr Res 1974 0.75
62 Population genetics and hemophilia--implications of mutation and carrier recognition. Ann N Y Acad Sci 1975 0.75
63 Semiautomatic digital printing caliper for tooth measurements. J Dent Res 1968 0.75
64 The linkage and mapping relationships of 1qh. Birth Defects Orig Artic Ser 1976 0.75