Maxine J. Sutcliffe

1.2k total citations
27 papers, 676 citations indexed

About

Maxine J. Sutcliffe is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maxine J. Sutcliffe has authored 27 papers receiving a total of 676 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maxine J. Sutcliffe's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Sperm and Testicular Function (4 papers). Maxine J. Sutcliffe is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Sperm and Testicular Function (4 papers). Maxine J. Sutcliffe collaborates with scholars based in United States, United Kingdom and Australia. Maxine J. Sutcliffe's co-authors include Paul S. Burgoyne, Shantha K. Mahadevaiah, Stephen J. Palmer, S.D.M. Brown, Jacquie T. Keer, Denise Y. P. Henriques, S. M. Darling, Hans‐Christoph Rossbach, Nyla A. Heerema and Jonathan J. Shuster and has published in prestigious journals such as Cell, Nature Genetics and Development.

In The Last Decade

Maxine J. Sutcliffe

27 papers receiving 654 citations

Peers

Countries citing papers authored by Maxine J. Sutcliffe

Since Specialization

Citations

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

Fields of papers citing papers by Maxine J. Sutcliffe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maxine J. Sutcliffe. 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 Maxine J. Sutcliffe. The network helps show where Maxine J. Sutcliffe may publish in the future.

Co-authorship network of co-authors of Maxine J. Sutcliffe

This figure shows the co-authorship network connecting the top 25 collaborators of Maxine J. Sutcliffe. A scholar is included among the top collaborators of Maxine J. Sutcliffe 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 Maxine J. Sutcliffe. Maxine J. Sutcliffe 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	The role of unpaired sex chromosomes in spermatogenic failure* 2009 ·Andrologia ·Paul S. Burgoyne, Maxine J. Sutcliffe, Shantha K. Mahadevaiah	5
2	A case study of “disorganized development” and its possible relevance to genetic determinants of aging 2009 ·Mechanisms of Ageing and Development ·Richard F. Walker, (unknown), Maxine J. Sutcliffe, Patricia A. Kruk, Jesper Graakjær, Jerry W. Shay	11
3	EXTREME VARIANT OF ENLARGED HETEROCHROMATIN REGION ON CHROMOSOME 9Q IN A NORMAL CHILD AND MULTIPLE FAMILY MEMBERS 2009 ·Fetal and Pediatric Pathology ·Thora S. Steffensen, Enid Gilbert‐Barness, Mary Sandstrom, JOHN R. BELL, (unknown), Maxine J. Sutcliffe	2
4	A patient with an interstitial duplication of chromosome 5p11–p13.3 further confirming a critical region for 5p duplication syndrome 2007 ·European Journal of Medical Genetics ·Melissa L. Loscalzo, (unknown), Maxine J. Sutcliffe	18
5	High concordance from independent studies by the Children's Cancer Group (CCG) and Pediatric Oncology Group (POG) associating favorable prognosis with combined trisomies 4, 10, and 17 in children with NCI Standard-Risk B-precursor Acute Lymphoblastic Leukemia: a Children's Oncology Group (COG) initiative 2005 ·Leukemia ·Maxine J. Sutcliffe, Jonathan J. Shuster, Harland N. Sather, Bruce M. Camitta, Jeanette Pullen, Kirk R. Schultz, M Borowitz, Paul S. Gaynon, Andrew J. Carroll, Nyla A. Heerema	88
6	Twin–twin transfusion syndrome in a dizygotic monochorionic–diamniotic twin pregnancy 2003 ·The Journal of Maternal-Fetal & Neonatal Medicine ·Rubén A. Quintero, O. Thomas Mueller, J. Martı́nez, Jorge Olmo Arroyo, Enid Gilbert‐Barness, Don R. Hilbelink, Peter Papenhausen, Maxine J. Sutcliffe	35
7	Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder 2003 ·Human Genetics ·Fiona Crawford, Ghania Ait‐Ghezala, Mark Morris, Maxine J. Sutcliffe, Robert A. Hauser, Archie A. Silver, Michael Mullan	19
8	Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX 2001 ·American Journal of Medical Genetics ·Maxine J. Sutcliffe, O. Thomas Mueller, Boris G. Kousseff, (unknown), (unknown), (unknown), (unknown), Judith D. Ranells	5
9	Pre-B Acute Lymphoblastic Leukemia in a 3-Year-Old Boy With Pre-Acute Myelogenous Leukemia Myelodysplastic Syndrome 1998 ·Journal of Pediatric Hematology/Oncology ·Hans‐Christoph Rossbach, Maxine J. Sutcliffe, (unknown), (unknown), (unknown), (unknown), (unknown)	8
10	Assignment<footref rid="foot01"><sup>1</sup></footref> of microsomal epoxide hydrolase (EPHX1) to human chromosome 1q42.1 by in situ hybridization 1998 ·Cytogenetic and Genome Research ·James K. Hartsfield, Maxine J. Sutcliffe, Eric T. Everett, Christopher Hassett, Curtis J. Omiecinski, (unknown)	28
11	Monosomy 6q1: Syndrome delineation 1996 ·American Journal of Medical Genetics ·(unknown), James K. Hartsfield, Maxine J. Sutcliffe, (unknown), Boris G. Kousseff	11
12	Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult 1996 ·American Journal of Medical Genetics ·Peter Papenhausen, O. Thomas Mueller, Maxine J. Sutcliffe, (unknown), Boris G. Kousseff, Virginia P. Johnson	8
13	Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome 1996 ·American Journal of Medical Genetics ·Hans‐Christoph Rossbach, Maxine J. Sutcliffe, (unknown), (unknown), (unknown), (unknown)	29
14	Recipient T‐Cell Immune Reconstitution in X‐linked SCID after Haploidentical Maternal Bone Marrow Transplant 1995 ·Annals of the New York Academy of Sciences ·M. Teresa de la Morena, A.S. Wayne, N K Day, (unknown), (unknown), R.P. Nelson, Maxine J. Sutcliffe, Robert A. Good	1
15	Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1 1992 ·Genomics ·Kathryn Brown, Maxine J. Sutcliffe, Karen P. Steel, S.D.M. Brown	17
16	Fertility in mice requires X-Y pairing and a Y-chromosomal “Spermiogenesis” gene mapping to the long arm 1992 ·Cell ·Paul S. Burgoyne, Shantha K. Mahadevaiah, Maxine J. Sutcliffe, Stephen J. Palmer	141
17	Mouse chromosome 7 1991 ·Mammalian Genome ·Eugene M. Rinchik, Ann M. Saunders, (unknown), Maxine J. Sutcliffe, Kathryn Brown, S.D.M. Brown, Josephine Peters	5
18	Spermatogenesis in XY, XYSxr^a and XOSxr^a mice: A quantitative analysis of spermatogenesis throughout puberty 1991 ·Molecular Reproduction and Development ·Maxine J. Sutcliffe, S. M. Darling, Paul S. Burgoyne	36
19	Reverse Genetic Approaches to Cloning Deafness Genes^a 1991 ·Annals of the New York Academy of Sciences ·S.D.M. Brown, Kathryn Brown, Maxine J. Sutcliffe, J. Cavanna, Andy Greenfield, Karen P. Steel	7
20	Analysis of the testes of H-Y negative XOSxrb mice suggests that the spermatogenesis gene (Spy) acts during the differentiation of the A spermatogonia 1989 ·Development ·Maxine J. Sutcliffe, Paul S. Burgoyne	79

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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