P R Papenhausen
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Explore the profile of P R Papenhausen including associated specialties, affiliations and a list of published articles.
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20
Citations
124
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Recent Articles
1.
Schwartz S, Kohan M, Pasion R, Papenhausen P, Platt L
Prenat Diagn
. 2018 Jan;
38(3):210-218.
PMID: 29338128
Objective: Screening via noninvasive prenatal testing (NIPT) involving the analysis of cell-free DNA (cfDNA) from plasma has become readily available to screen for chromosomal and DNA aberrations through maternal blood....
2.
Burnside R, Ibrahim J, Flora C, Schwartz S, Tepperberg J, Papenhausen P, et al.
Cytogenet Genome Res
. 2011 Jan;
132(4):227-32.
PMID: 21212645
Background/aims: The 'McClintock mechanism' of chromosome breakage and centromere misdivision, in which a deleted chromosome with its concomitant excised marker or ring chromosome is formed, has been described in approximately...
3.
Murphy S, Wylie A, Coveler K, Cotter P, Papenhausen P, Sutton V, et al.
Hum Mutat
. 2003 Jun;
22(1):92-7.
PMID: 12815599
The recent demonstration of genomic imprinting of DLK1 and MEG3 on human chromosome 14q32 indicates that these genes might contribute to the discordant phenotypes associated with uniparental disomy (UPD) of...
4.
Reddy P, Papenhausen P, Suh Y, Riddick L, Calvano C, MANDELL J
J Urol
. 1997 Sep;
158(3 Pt 2):1305-7.
PMID: 9258201
Purpose: The mammalian sex determining gene, sex region Y chromosome (SRY), is now firmly established as the testis determining locus. The SRY locus is close to the short arm Y...
5.
Becker J, Papenhausen P, Widen R
In Vitro Cell Dev Biol Anim
. 1997 May;
33(5):325-31.
PMID: 9196889
A cell line was established from a mixed mullerian tumor of the ovary and designated LN1. Histopathologic analysis of the fresh tumor specimen demonstrated a highly aneuploid heterologous tumor comprised...
6.
Papenhausen P, Mueller O, Sutcliffe M, Diamond T, Kousseff B, Johnson V
Am J Med Genet
. 1996 Dec;
66(1):90.
PMID: 8957521
No abstract available.
7.
Joseph M, Cantu E, Pai G, Willi S, Papenhausen P, WEISS L
J Med Genet
. 1996 Nov;
33(11):906-11.
PMID: 8950669
Colony stimulating factor-2 receptor alpha (CSF2RA) and interleukin-3 receptor alpha (IL3RA), two genes from the chromosome Xp and Yp pseudoautosomal region (PAR), have been suggested as candidate genes for short...
8.
Rogan P, Seip J, Driscoll D, Papenhausen P, Johnson V, Raskin S, et al.
Am J Med Genet
. 1996 Mar;
62(1):10-5.
PMID: 8779316
Individuals with a ring 15 chromosome [r(15)] and those with Russell-Silver syndrome have short stature, developmental delay, triangular face, and clinodactyly. To assess whether the apparent phenotypic overlap of these...
9.
Papenhausen P, Mueller O, Johnson V, Sutcliffe M, Diamond T, Kousseff B
Am J Med Genet
. 1995 Nov;
59(3):271-5.
PMID: 8599348
Uniparental disomy (UPD) of a number of different chromosomes has been found in associated with abnormal phenotypes. A growing body of evidence for an imprinting effect involving chromosome 14 has...
10.
Agaliotis D, Papenhausen P, Moscinski L, Elfenbein G
Ann Hematol
. 1995 Jan;
70(1):37-41.
PMID: 7827205
Detection of the chronic myelogenous leukemia (CML)-related marker, the bcr/abl m-RNA transcript, in blood or bone marrow of patients with CML in hematologic remission after allogeneic bone marrow transplantation (allo-BMT)...