P. N. Howard‐Peebles
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- Prenatal Screening and Diagnostics 6
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 6
- Genetic Syndromes and Imprinting 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Obstetrics and Gynecology top 10%
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- Congenital heart defects research 2
- Genomics and Chromatin Dynamics 2
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- Chromosomal and Genetic Variations 4
- Co-authors
- Dagmar K. KalousekIrene BarrettSylvie LangloisR. Douglas WilsonL.E. BernardWendy P. RobinsonAdèle TeleniusAndrew Dorfmann
- Journals
- Molecular and Cellular Biology (1 paper)The American Journal of Human Genetics (1 paper)American Journal of Medical Genetics (5 papers)
- Partner nations
- United StatesCanada
In The Last Decade
P. N. Howard‐Peebles
15 papers receiving 761 citations
Peers
Comparison fields: 5 of 41
- Pediatrics, Perinatology and Child Health 513
- Genetics 566
- Obstetrics and Gynecology 49
- Developmental Biology 10
- Molecular Biology 293
Countries citing papers authored by P. N. Howard‐Peebles
This map shows the geographic impact of P. N. Howard‐Peebles'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 P. N. Howard‐Peebles with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. N. Howard‐Peebles more than expected).
Fields of papers citing papers by P. N. Howard‐Peebles
This network shows the impact of papers produced by P. N. Howard‐Peebles. 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 P. N. Howard‐Peebles. The network helps show where P. N. Howard‐Peebles may publish in the future.
Co-authorship network
The 25 scholars most cited alongside P. N. Howard‐Peebles, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 18 | |
| 2 | Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. | 1997 | 164 |
| 3 | Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study | 1997 | 0 |
| 4 | 1996 | 46 | |
| 5 | The fragile X premutation in carriers and its effect on mutation size in offspring. | 1995 | 53 |
| 6 | Uniparental disomy for chromosome 16 in humans. | 1993 | 155 |
| 7 | 1992 | 13 | |
| 8 | 1991 | 153 | |
| 9 | 1990 | 52 | |
| 10 | Chorionic villus sampling mosaicism: counseling issues. | 1990 | 1 |
| 11 | 1988 | 5 | |
| 12 | 1986 | 67 | |
| 13 | 1983 | 8 | |
| 14 | 1983 | 31 | |
| 15 | 1981 | 5 | |
| 16 | Partial trisomy of chromosome 15. | 1977 | 7 |
About P. N. Howard‐Peebles
P. N. Howard‐Peebles is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Obstetrics and Gynecology, having authored 16 papers that have together received 778 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (4 papers), Chromosomal and Genetic Variations (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Congenital heart defects research (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (513 citations), Genetics (566 citations) and Obstetrics and Gynecology (49 citations). P. N. Howard‐Peebles has collaborated with scholars based in United States and Canada. Frequent co-authors include Dagmar K. Kalousek, Irene Barrett, Sylvie Langlois, R. Douglas Wilson, L.E. Bernard, Wendy P. Robinson, Adèle Telenius, Andrew Dorfmann, Debra Rose Wilson and Susan B. Olson. Their work appears in journals such as Molecular and Cellular Biology, The American Journal of Human Genetics and American Journal of Medical Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.