The University of Chicago Header Logo

Connection

Michael Z. Ludwig to Humans

This is a "connection" page, showing publications Michael Z. Ludwig has written about Humans.
Connection Strength

0.119
  1. An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome. Int J Mol Med. 2013 Jul; 32(1):174-8.
    View in: PubMed
    Score: 0.014
  2. Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variant. Kidney Blood Press Res. 2003; 26(3):176-84.
    View in: PubMed
    Score: 0.007
  3. Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadias. Scand J Urol Nephrol. 2003; 37(6):498-501.
    View in: PubMed
    Score: 0.007
  4. A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length? Hum Genet. 2002 May; 110(5):488-94.
    View in: PubMed
    Score: 0.007
  5. Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PLoS One. 2020; 15(6):e0234246.
    View in: PubMed
    Score: 0.006
  6. The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia. Nat Struct Biol. 1999 Apr; 6(4):359-65.
    View in: PubMed
    Score: 0.005
  7. Autophagy Inhibition Mediates Apoptosis Sensitization in Cancer Therapy by Relieving FOXO3a Turnover. Dev Cell. 2018 03 12; 44(5):555-565.e3.
    View in: PubMed
    Score: 0.005
  8. ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development. Sci Rep. 2017 02 08; 7:42170.
    View in: PubMed
    Score: 0.005
  9. Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatr Genet. 2016 12; 26(6):293-296.
    View in: PubMed
    Score: 0.005
  10. Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase. Proc Natl Acad Sci U S A. 1996 May 28; 93(11):5550-5.
    View in: PubMed
    Score: 0.004
  11. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Hum Mutat. 2015 Dec; 36(12):1150-4.
    View in: PubMed
    Score: 0.004
  12. WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish. Hum Mol Genet. 2015 Sep 15; 24(18):5069-78.
    View in: PubMed
    Score: 0.004
  13. Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy. PLoS Genet. 2015 Mar; 11(3):e1005024.
    View in: PubMed
    Score: 0.004
  14. Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Hum Mol Genet. 2014 Oct 15; 23(20):5536-44.
    View in: PubMed
    Score: 0.004
  15. Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):512-7.
    View in: PubMed
    Score: 0.004
  16. Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin. Genetics. 2014 Feb; 196(2):539-55.
    View in: PubMed
    Score: 0.004
  17. Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. Genetics. 2014 Feb; 196(2):557-67.
    View in: PubMed
    Score: 0.004
  18. VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol. 2012 Oct; 21(4):191-195.
    View in: PubMed
    Score: 0.003
  19. Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias. Gene. 2012 Sep 15; 506(2):392-5.
    View in: PubMed
    Score: 0.003
  20. Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Am J Hum Genet. 2011 Nov 11; 89(5):668-74.
    View in: PubMed
    Score: 0.003
  21. p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissue. Int J Mol Med. 2010 Dec; 26(6):861-7.
    View in: PubMed
    Score: 0.003
  22. Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias. Birth Defects Res A Clin Mol Teratol. 2010 Jul; 88(7):546-50.
    View in: PubMed
    Score: 0.003
  23. Analysis of Drosophila segmentation network identifies a JNK pathway factor overexpressed in kidney cancer. Science. 2009 Feb 27; 323(5918):1218-22.
    View in: PubMed
    Score: 0.003
  24. Low frequency of imprinting defects in ICSI children born small for gestational age. Eur J Hum Genet. 2009 Jan; 17(1):22-9.
    View in: PubMed
    Score: 0.003
  25. R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasia. Pediatr Nephrol. 2005 Dec; 20(12):1724-8.
    View in: PubMed
    Score: 0.002
  26. Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Hum Mol Genet. 2004 Nov 15; 13(22):2841-51.
    View in: PubMed
    Score: 0.002
  27. Emergence of epidemic O'nyong-nyong fever in Uganda after a 35-year absence: genetic characterization of the virus. Virology. 1998 Dec 05; 252(1):258-68.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.