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KYLE KUTSCHE, MD
MD
Sports Medicine (Family Medicine) Physician
NPI: 1790047918IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine Physician
Family Medicine
Code: 207Q00000X
27602(NE)
Sports Medicine (Family Medicine) PhysicianPrimary
Family Medicine — Sports Medicine
Code: 207QS0010X
0101264969(VA)4301506248(MI)
Education
MICHIGAN STATE UNIVERSITY COLLEGE OF HUMAN MEDICINE
Class of 2012
Research & Publications (20)
Oncogenic HRAS mutations cause prolonged PI3K signaling in response to epidermal growth factor in fibroblasts of patients with Costello syndrome.
PMID 19035362·Hum Mutat·2009
8-other
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
PMID 19277062·Eur J Hum Genet·2009
8-other
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
PMID 18541964·Clin Dysmorphol·2008
8-other
AlphaPIX Rho GTPase guanine nucleotide exchange factor regulates lymphocyte functions and antigen receptor signaling.
PMID 18378701·Mol Cell Biol·2008
7-preclinical
Disruption of neurexin 1 associated with autism spectrum disorder.
PMID 18179900·Am J Hum Genet·2008
8-other
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
PMID 18042262·Clin Genet·2008
8-other
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum.
PMID 19165920·Nat Genet·2008
8-other
Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.
PMID 18954413·Clin Genet·2008
8-other
Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
PMID 17937436·Am J Med Genet A·2007
8-other
HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?
PMID 17893649·Mol Vis·2007
7-preclinical
SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome.
PMID 17586837·J Med Genet·2007
8-other
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.
PMID 17056636·J Med Genet·2007
8-other
A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
PMID 17033686·Eur J Hum Genet·2007
5-case
AlphaPIX and betaPIX and their role in focal adhesion formation.
PMID 16337026·Eur J Cell Biol·2006
6-review
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.
PMID 17033964·Am J Hum Genet·2006
5-case
PAK4 and alphaPIX determine podosome size and number in macrophages through localized actin regulation.
PMID 16897755·J Cell Physiol·2006
8-other
The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody.
PMID 16406728·Genomics·2006
8-other
Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome.
PMID 15770227·Eur J Hum Genet·2005
5-case
Disruption of ERBB2IP is not associated with dystrophic epidermolysis bullosa in both father and son carrying a balanced 5;13 translocation.
PMID 16185268·J Invest Dermatol·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3443 FARR RD
FRUITPORT, MI 49415 - Phone
- (231) 672-2900
Quick Facts
- NPI
- 1790047918
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 14
- Publications
- 20
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