K Falls
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Explore the profile of K Falls including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
70
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Recent Articles
1.
Van Eerdewegh P, Dowd M, Dupuis J, Falls K, Hayward B, Santangelo S
Genet Epidemiol
. 2002 Jan;
21 Suppl 1:S67-72.
PMID: 11793760
We contrast the pooling of multiple data sets with the compound HLOD (HLOD-C) and the posterior probability of linkage (PPL), two approaches that have been shown to have more power...
2.
Bertram L, Hayward B, Lake S, Falls K, Van Erdewegh P, Blacker D
Genet Epidemiol
. 2002 Jan;
21 Suppl 1:S292-7.
PMID: 11793685
Correlation among sibling marker genotypes may invalidate the results of family-based tests of association in the presence of linkage. We apply an empirical variance estimation method, which is implemented in...
3.
Smith D, Richterich P, Rubenfield M, Rice P, Butler C, Lee H, et al.
Genome Res
. 1997 Aug;
7(8):802-19.
PMID: 9267804
The nucleotide sequence of 1.5 Mb of genomic DNA from Mycobacterium leprae was determined using computer-assisted multiplex sequencing technology. This brings the 2.8-Mb M. leprae genome sequence to approximately 66%...
4.
Ting C, Burgess D, Chamberlain J, Keith T, Falls K, Meisler M
Genomics
. 1993 Jun;
16(3):698-706.
PMID: 8325643
The human PCK1 gene encoding phosphoenolpyruvate carboxykinase (GTP) (PEPCK) was isolated and sequenced. There is 91% amino acid sequence identity (567/622 residues) between the human and the rat proteins, with...
5.
Ginns E, Egeland J, Allen C, Pauls D, Falls K, Keith T, et al.
J Psychiatr Res
. 1992 Oct;
26(4):305-8.
PMID: 1362775
In this report we describe our efforts to identify a gene involved in bipolar illness using a large, multigenerational Old Order Amish pedigree with many affected individuals. The original collection...
6.
Weiffenbach B, Bagley R, Falls K, Hyser C, Storvick D, Jacobsen S, et al.
Am J Hum Genet
. 1992 Aug;
51(2):416-23.
PMID: 1642240
The genetic locus for facioscapulohumeral muscular dystrophy (FSHD) has been mapped to chromosome 4. We have examined linkage to five chromosome 4q DNA markers in 22 multigenerational FSHD families. Multipoint...
7.
Weiffenbach B, Bagley R, Falls K, Dubois J, Hyser C, Storvick D, et al.
Mamm Genome
. 1992 Jan;
3(3):143-50.
PMID: 1352159
Mapping the long arm of Chromosome (Chr) 4 has assumed medical relevance with the establishment of linkage of facioscapulohumeral muscular dystrophy (FSHD) to distal 4q markers. We have constructed a...
8.
Olschwang S, Weiffenbach B, Laurent-Puig P, Melot T, Vassal A, Falls K, et al.
Gastroenterology
. 1991 Jul;
101(1):154-60.
PMID: 1646139
Familial adenomatous polyposis is a rare disease inherited in a Mendelian dominant fashion. It is characterized by the occurrence of more than 100 adenomatous polyps in the large bowels of...
9.
Weiffenbach B, Falls K, Bricker A, Hall L, McMahon J, Wasmuth J, et al.
Genomics
. 1991 May;
10(1):173-85.
PMID: 1675192
A genetic map of human chromosome 5 that contains 60 restriction fragment length polymorphism (RFLP) loci in one linkage group has been constructed. Segregation data using these markers and 40...
10.
Jacobsen S, Diala E, Dorsey B, Rising M, Graveline R, Falls K, et al.
Am J Hum Genet
. 1990 Sep;
47(3):376-88.
PMID: 1975474
Facioscapulohumeral muscular dystrophy (FSHMD) is a neuromuscular disorder characterized by autosomal dominant inheritance and clinical onset in the muscles of the face and shoulder girdle. Using a set of RFLP...