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WHITNEY KRESS, M.D.
M.D.
Internal Medicine Physician
NPI: 1376980128IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
256586(MA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
YALE UNIVERSITY SCHOOL OF MEDICINE
Class of 2013
Research & Publications (20)
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
PMID 16251895·Eur J Hum Genet·2006
8-other
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).
PMID 10996776·Neuromuscul Disord·2000
8-other
Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).
PMID 11173845·Cytogenet Cell Genet·2000
8-other
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.
PMID 11173846·Cytogenet Cell Genet·2000
5-case
Sustained platelet-derived growth factor receptor alpha signaling in osteoblasts results in craniosynostosis by overactivating the phospholipase C-gamma pathway.
PMID 19047372·Mol Cell Biol·2009
7-preclinical
Boy with pseudohypoparathyroidism type 1a caused by GNAS gene mutation (deltaN377), Crouzon-like craniosynostosis, and severe trauma-induced bleeding.
PMID 19530187·Am J Med Genet A·2009
5-case
Controlled destruction: AAA+ ATPases in protein degradation from bacteria to eukaryotes.
PMID 19362814·Curr Opin Struct Biol·2009
6-review
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1.
PMID 19006247·Hum Mutat·2009
7-preclinical
Studying chaperone-proteases using a real-time approach based on FRET.
PMID 19591940·J Struct Biol·2009
8-other
Intersubunit cross-talk in pyridoxal 5'-phosphate synthase, coordinated by the C terminus of the synthase subunit.
PMID 19074821·J Biol Chem·2009
8-other
Effect of flower shape and size on foraging performance and trade-offs in a tropical hummingbird.
PMID 19537537·Ecology·2009
7-preclinical
The flexible attachment of the N-domains to the ClpA ring body allows their use on demand.
PMID 18358489·J Mol Biol·2008
8-other
Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy.
PMID 18348272·Am J Med Genet A·2008
5-case
DNA barcodes: genes, genomics, and bioinformatics.
PMID 18287050·Proc Natl Acad Sci U S A·2008
8-other
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.
PMID 18684626·Neuromuscul Disord·2008
5-case
PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.
PMID 19061984·Am J Hum Genet·2008
8-other
Late onset in dysferlinopathy widens the clinical spectrum.
PMID 18396043·Neuromuscul Disord·2008
5-case
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.
PMID 18807109·J Neurol·2008
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
- 978 WORCESTER ST FL 2
WELLESLEY, MA 02482 - Phone
- (781) 235-5200
Quick Facts
- NPI
- 1376980128
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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