Annette E. Cockwell

1.5k total citations
25 papers, 903 citations indexed

About

Annette E. Cockwell is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Annette E. Cockwell has authored 25 papers receiving a total of 903 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 11 papers in Molecular Biology. Recurrent topics in Annette E. Cockwell's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (8 papers). Annette E. Cockwell is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (8 papers). Annette E. Cockwell collaborates with scholars based in United Kingdom, United States and Canada. Annette E. Cockwell's co-authors include P. A. Jacobs, John A. Crolla, I. Karen Temple, Terry Hassold, Dorothy Pettay, Matthew Mackenzie, Sheila Youings, Andrew Fisher, Patricia A. Jacobs and Amanda Collins and has published in prestigious journals such as Developmental Medicine & Child Neurology, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Annette E. Cockwell

25 papers receiving 843 citations

Peers

Countries citing papers authored by Annette E. Cockwell

Since Specialization

Citations

This map shows the geographic impact of Annette E. Cockwell'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 Annette E. Cockwell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annette E. Cockwell more than expected).

Fields of papers citing papers by Annette E. Cockwell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Annette E. Cockwell. 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 Annette E. Cockwell. The network helps show where Annette E. Cockwell may publish in the future.

Co-authorship network of co-authors of Annette E. Cockwell

This figure shows the co-authorship network connecting the top 25 collaborators of Annette E. Cockwell. A scholar is included among the top collaborators of Annette E. Cockwell based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Annette E. Cockwell. Annette E. Cockwell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Investigation of the origins of human autosomal inversions 2008 ·Human Genetics ·N. Simon Thomas, Victoria Bryant, V.K. Maloney, Annette E. Cockwell, Patricia A. Jacobs	17
2	Distribution of the D15Z1 copy number polymorphism 2007 ·European Journal of Human Genetics ·Annette E. Cockwell, Patricia A. Jacobs, John A. Crolla	12
3	The origin of trisomy 13 2007 ·American Journal of Medical Genetics Part A ·(unknown), E. Ricky Chan, Andrew Collins, LuAnn Judis, (unknown), Urvashi Surti, Lori Hoffner, Annette E. Cockwell, Patricia A. Jacobs, Terry Hassold	23
4	Mosaic trisomy 6 and maternal uniparental disomy 6 in a 23‐week gestation fetus with atrioventricular septal defect 2006 ·American Journal of Medical Genetics Part A ·Annette E. Cockwell, Samantha Baker, (unknown), Isabella Moore, John A. Crolla	25
5	Nondisjunction of chromosome 21 2005 ·American Journal of Medical Genetics ·Norma T. Takaesu, Patricia A. Jacobs, Annette E. Cockwell, R. Dwain Blackston, Sallie B. Freeman, (unknown), David M. Kurnit, Irene A. Uchida, Viola Freeman, Terry Hassold	15
6	Pallister–Killian syndrome: an unusual cause of epileptic spasms 2005 ·Developmental Medicine & Child Neurology ·Rocío Sánchez‐Carpintero, Ailsa McLellan, Lucio Parmeggiani, Annette E. Cockwell, Richard J. Ellis, J. Helen Cross, (unknown), Renzo Guerrini	8
7	Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalities 2005 ·Cytogenetic and Genome Research ·Annette E. Cockwell, V. Maloney, N S Thomas, (unknown), (unknown), Paul Bass, John A. Crolla	2
8	Pallister—Killian syndrome: an unusual cause of epileptic spasms 2005 ·Developmental Medicine & Child Neurology ·Rocío Sánchez‐Carpintero, Ailsa McLellan, Lucio Parmeggiani, Annette E. Cockwell, Richard J. Ellis, J. Helen Cross, (unknown), Renzo Guerrini	1
9	A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities 2003 ·Human Genetics ·Annette E. Cockwell, Patricia A. Jacobs, Sarah J. Beal, John A. Crolla	28
10	Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation 2002 ·Human Genetics ·Andrew Fisher, Simon Thomas, Annette E. Cockwell, (unknown), Bronwyn Kerr, I. Karen Temple, Peter Clayton	76
11	Centromeric inactivation in a dicentric human Y;21 translocation chromosome 1997 ·Chromosoma ·Andrew Fisher, Lihadh Al‐Gazali, (unknown), (unknown), Annette E. Cockwell, John Barber, William C. Earnshaw, Joyce Axelman, Barbara R. Migeon, Chris Tyler‐Smith	32
12	RAPIDIN SITU HARVESTING AND CYTOGENETIC ANALYSIS OF PERINATAL TISSUE SAMPLES 1996 ·Prenatal Diagnosis ·Andrew Fisher, Annette E. Cockwell, (unknown), N. Gregson, Paul L. Campbell, (unknown), (unknown), John Barber, John A. Crolla	11
13	A CASE OF MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 9 IN ASSOCIATION WITH CONFINED PLACENTAL MOSAICISM FOR TRISOMY 9 1996 ·Prenatal Diagnosis ·(unknown), (unknown), (unknown), Annette E. Cockwell, (unknown), (unknown)	24
14	Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23). 1996 ·Journal of Medical Genetics ·Annette E. Cockwell, R S James, Isabella Moore, Eli Hatchwell, John A. Crolla	13
15	Incidence of circulating cells positive for GpIb and GpIIIa in infants with Down's syndrome 1994 ·European Journal Of Haematology ·Andrew Fisher, Annette E. Cockwell, P. A. Jacobs, Hugh Parry	2
16	Three patients with ring (X) chromosomes and a severe phenotype. 1993 ·Journal of Medical Genetics ·N R Dennis, Amanda Collins, John A. Crolla, Annette E. Cockwell, Andrew Fisher, P. A. Jacobs	72
17	Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia 1992 ·Genes Chromosomes and Cancer ·(unknown), Sallie B. Freeman, Terry Hassold, Abdel Ragab, Roger A. Vega, Annette E. Cockwell, Patricia A. Jacobs, (unknown), (unknown), Ian D. Dubé, Alvin Zipursky	17
18	Maternal uniparental disomy for chromosome 14. 1991 ·Journal of Medical Genetics ·I. Karen Temple, Annette E. Cockwell, Terry Hassold, Dorothy Pettay, (unknown)	154
19	Trisomy 21: association between reduced recombination and nondisjunction. 1991 ·PubMed ·Stephanie L. Sherman, Norma T. Takaesu, Sallie B. Freeman, (unknown), Charlotte Phillips, R. Dwain Blackston, P. A. Jacobs, Annette E. Cockwell, Viola Freeman, Irene A. Uchida	139
20	A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome 1990 ·Annals of Human Genetics ·P. A. Jacobs, P R Betts, Annette E. Cockwell, John A. Crolla, Matthew Mackenzie, David Robinson, Sheila Youings	90

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.

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