Philip N. Mowrey

627 citations

22 papers · 436 indexed · h-index 11

Genetics top 10%
- Genomic variations and chromosomal abnormalities 10
- Chronic Lymphocytic Leukemia Research 3
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics 5
Developmental Biology
- Congenital limb and hand anomalies 2
Genetics
- Genomic variations and chromosomal abnormalities 10
- Chronic Lymphocytic Leukemia Research 3
Hematology
- Acute Myeloid Leukemia Research 5
- Chronic Myeloid Leukemia Treatments 4
Plant Science
- Chromosomal and Genetic Variations 3
Molecular Biology
- RNA regulation and disease 2

Co-authors: Richard C. Juberg Roger L. Ladda Jeanette C. Ramer Geoffrey Miller David Robins Kenneth D. Hopper Javad Towfighi JoAnn C. Kelly
Cited by: Genetics Pediatrics, Perinatology and Child Health Developmental Biology
Journals: Journal of Medical Genetics (2 papers)Molecular Cytogenetics (1 paper)Clinical Genetics (1 paper)
Partner nations: United States United Kingdom Italy

In The Last Decade

Philip N. Mowrey

21 papers receiving 415 citations

Peers

Countries citing papers authored by Philip N. Mowrey

Since Specialization

Citations

This map shows the geographic impact of Philip N. Mowrey's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Philip N. Mowrey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philip N. Mowrey more than expected).

Fields of papers citing papers by Philip N. Mowrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip N. Mowrey. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Philip N. Mowrey. The network helps show where Philip N. Mowrey may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Philip N. Mowrey, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Philip N. Mowrey Line = papers co-authored together Philip N. Mowrey links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Deletions of the PRKAR1A Locus at 17q24.2-q24.3 in Carney Complex: Genotype-Phenotype Correlations and Implications for Genetic Testing The Journal of Clinical Endocrinology & Metabolism ·(unknown),Anélia Horvath,Edra London,Fábio R. Faucz,Annalisa Vetro,Isaac Lévy,Evgenia Gourgari,Andrew Dauber,Ingrid A. Holm,Patrick J. Morrison,Margaret F. Keil,Charalampos Lyssikatos,Eric D. Smith,Ekrem Bektašević,JoAnn C. Kelly,Zunyan Dai,Philip N. Mowrey,Antonella Forlino,Orsetta Zuffardi,Constantine A. Stratakis	2013	51
2	Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas Molecular Cytogenetics ·Zunyan Dai,JoAnn C. Kelly,Aurelia Meloni‐Ehrig,Marilyn L. Slovak,D.S. Best,Thais Gomes Araújo Sousa,Christine R. Bryke,Steven Schonberg,Лукьянова Ирина Геннадьевна,Qiulu Pan,Albert K. Ho,Heather Sanders,Kostiantyn Khadartsev,Dan Jones,Philip N. Mowrey	2012	26
3	Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia Cancer Genetics and Cytogenetics ·JoAnn C. Kelly,Tadashi Kudo,A A Mukhametgalina,G. Heberer,雨张,Thais Gomes Araújo Sousa,Philip N. Mowrey,Rocky O'Donovan,Virginia Dodier,Aurelia Meloni‐Ehrig	2009	19
4	Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation Cancer Genetics and Cytogenetics ·Gulsun Erdag,Jeanne Meck,Aurelia Meloni‐Ehrig,Ludmila Matyakhina,Zi Yun Li,Ramaprasad Srinivasan,Philip N. Mowrey,Fumiya Oshika,G. A. Kochetova,Richard Childs	2009	3
5	Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma Cancer Genetics and Cytogenetics ·Aurelia Meloni‐Ehrig,张春竹,Nicole Farrow,Anthony J. Crispino,周惠芬,Syed M. A. Zaman,Philip N. Mowrey	2009	11
6	Stimulation of B-Cell Mature Malignancies with the CpG-Oligonucleotide DSP30 and Interleukin-2 for Improved Detection of Chromosome Abnormalities. Blood ·Aurelia Meloni‐Ehrig,Jeanne Meck,Thais Gomes Araújo Sousa,JoAnn C. Kelly,Ludmila Matyakhina,Steven Schonberg,Zulfiya Makhmudovna Abdulaeva,Muhammad-Baqir Muhammad-Rashad Fakhrildin,Razieh Montazerfaraj,Steven L. Gersen,Yaris Setiabudi,Michael Ho-Chang Chae,Lisa L. Brailey,T. F. HARRISS,N. Markard,Tadashi Kudo,河本正次,Rafael Sirera,Philip N. Mowrey	2009	1
7	Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case Cancer Genetics and Cytogenetics ·Carlos A Tirado,Aurelia Meloni‐Ehrig,Govindharajulu Jeevan Prasaad,A A Mukhametgalina,William Shibuya,Paloma Marques Alves,Thais Gomes Araújo Sousa,Tatiana Melissa,Jared A. Greenberg,Clifton N. Murphy,河本正次,Chetan Vikram Andhare,Philip N. Mowrey	2007	3
8	Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies Cancer Genetics and Cytogenetics ·Carlos A Tirado,Aurelia Meloni‐Ehrig,Yong Feng Zhou,William Shibuya,A A Mukhametgalina,Marzieh Khodaei Goki,JoAnn C. Kelly,飯塚哲太郎,Alexander I. Spira,河本正次,Lewis Glasser,James N. Butera,Philip N. Mowrey	2006	0
9	Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion Cancer Genetics and Cytogenetics ·Carlos A Tirado,G. Heberer,A A Mukhametgalina,Deepali B. Khot,Robert J. Meister,Robert Christie,河本正次,Abbas Antsar Ahmed Abbas,Chetan Vikram Andhare,Philip N. Mowrey,Aurelia Meloni‐Ehrig	2005	5
10	Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia Cancer Genetics and Cytogenetics ·Aurelia Meloni‐Ehrig,Carlos A Tirado,Hussein Rabee Humadi,G. Heberer,V. E. Petrashen,A A Mukhametgalina,D Kimibiris,Holly J. Meany,Wefky Elsayed,David Leitenberg,飯塚哲太郎,Philip N. Mowrey	2005	1
11	Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH American Journal of Medical Genetics ·Mark J. Pettenati,Sociedad de Comunicaciones,Bev Braune,William Stewart,C. Von Kap-Herr,Philip N. Mowrey,P. Nagesh Rao,Kristin M. May	2002	6
12	Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes Prenatal Diagnosis ·Mark J. Pettenati,C. Von Kap-Herr,Sociedad de Comunicaciones,Bev Braune,Philip N. Mowrey,Stuart Schwartz,P. Nagesh Rao,SHAWN T. LYONS	2002	24
13	Molecularly defined interstitial tandem duplication 6p case with mild manifestations American Journal of Medical Genetics ·Huazhen Fang,Philip N. Mowrey,Jiannis Ragoussis,Ghazala Mirza,Si ok Ryu,Adil Aman,Clesson Turner,Sondra W. Levin	2001	18
14	Clinical and molecular analyses of deletion 3p25‐pter syndrome American Journal of Medical Genetics ·Philip N. Mowrey,Michael J. Chorney,Charles P. Venditti,Farida Latif,William S. Modi,Michael I. Lerman,Berton Zbar,David Robins,Peter K. Rogan,Roger L. Ladda	1993	37
15	Malformations in a child with dup (7 pter‐p15.1) and del (7 q36‐qter) as a result of familial pericentric inversion Clinical Genetics ·Jeanette C. Ramer,Philip N. Mowrey,Roger L. Ladda	1991	10
16	Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: Review of brain, cardiac, and limb malformations American Journal of Medical Genetics ·Jeanette C. Ramer,Philip N. Mowrey,David Robins,Roger Springthorpe,Javad Towfighi,Jennifer Wozniczka	1990	57
17	Neurologic manifestations in 18q– syndrome American Journal of Medical Genetics ·Geoffrey Miller,Philip N. Mowrey,Kenneth D. Hopper,Matteo Ciniselli,Roger L. Ladda	1990	63
18	Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous aborters. Journal of Medical Genetics ·Richard C. Juberg,G. Gridel,Philip N. Mowrey	1985	16
19	Interstitial del(13q) associated with blindness and mental retardation American Journal of Medical Genetics ·Richard C. Juberg,Philip N. Mowrey,John M. Opitz	1984	6
20	Origin of nondisjunction in trisomy 21 syndrome: All studies compiled, parental age analysis, and international comparisons American Journal of Medical Genetics ·Richard C. Juberg,Philip N. Mowrey	1983	73

About Philip N. Mowrey

Philip N. Mowrey is a scholar working on Developmental Biology, Hematology and Genetics, having authored 22 papers that have together received 436 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Acute Myeloid Leukemia Research (5 papers), Prenatal Screening and Diagnostics (5 papers), Chronic Myeloid Leukemia Treatments (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Chromosomal and Genetic Variations (3 papers), Congenital limb and hand anomalies (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Genetics (232 citations), Pediatrics, Perinatology and Child Health (134 citations) and Developmental Biology (13 citations). Philip N. Mowrey has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Richard C. Juberg, Roger L. Ladda, Jeanette C. Ramer, Geoffrey Miller, David Robins, Kenneth D. Hopper, Javad Towfighi, JoAnn C. Kelly, Aurelia Meloni‐Ehrig and Farida Latif. Their work appears in journals such as Journal of Medical Genetics, Molecular Cytogenetics, Clinical Genetics, Human Genetics and Prenatal Diagnosis.

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