Maureen Bocian

3.6k citations

35 papers · 2.1k indexed · 1 hit paper · h-index 18

Genetics top 1%
Molecular Biology top 10%
Surgery
Pediatrics, Perinatology and Child Health top 5%
Cognitive Neuroscience top 10%

Co-authors: John J. Wasmuth Rita Shiang Deanna M. Church Thomas J. Fielder Yazhen Zhu Leslie M. Thompson Sara T. Winokur John M. Opitz
Topics: Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (8 papers)Connective tissue disorders research (4 papers)
Cited by: Genetics Developmental Biology Molecular Biology
Journals: Cell Annals of Neurology Genome Research
Partner nations: United States United Kingdom Japan

In The Last Decade

Maureen Bocian

35 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

1994 988 citations Rita Shiang, Deanna M. Church et al. profile →

Peers

Countries citing papers authored by Maureen Bocian

Since Specialization

Citations

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

Fields of papers citing papers by Maureen Bocian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maureen Bocian. 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 Maureen Bocian. The network helps show where Maureen Bocian may publish in the future.

Co-authorship network of co-authors of Maureen Bocian

This figure shows the co-authorship network connecting the top 25 collaborators of Maureen Bocian. A scholar is included among the top collaborators of Maureen Bocian 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 Maureen Bocian. Maureen Bocian 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	Computed tomographic reconstruction of a fetus with the dysgnathia complex (agnathia‐otocephaly) 2006 ·Prenatal Diagnosis ·Priya Rajan,Deborah A. Wing,Maureen Bocian,(unknown)	8
2	Preconception and prenatal testing of biologic fathers for carrier status 2006 ·Genetics in Medicine ·Beth A. Pletcher,Maureen Bocian	14
3	A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R 2004 ·BMC Medical Genetics ·(unknown),Abigail Woodroffe,Pamela Flodman,(unknown),(unknown),Charlotte Modahl,Robin Steinberg-Epstein,Maureen Bocian,M. Anne Spence,Moyra Smith	72
4	Mitochondrial dysfunction in autistic patients with 15q inverted duplication 2003 ·Annals of Neurology ·Pauline A. Filipek,(unknown),Moyra Smith,(unknown),(unknown),Maureen Bocian,Diane Masser‐Frye,Tracy M. Laulhere,Charlotte Modahl,M. Anne Spence,J. Jay Gargus	109
5	Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation 2003 ·Journal of Inherited Metabolic Disease ·J. Jay Gargus,(unknown),Maureen Bocian,Diane S. Roe,Christine Vianey‐Saban,Charles R. Roe	13
6	Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits 2002 ·Cytogenetic and Genome Research ·M. Smith,Abigail Woodroffe,(unknown),(unknown),Josefina Lozano Martínez,Pauline A. Filipek,Charlotte Modahl,B. P. L. Moore,Maureen Bocian,(unknown),Tracy M. Laulhere,Pamela Flodman,M. Anne Spence	40
7	Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR 2001 ·Cytogenetic and Genome Research ·M. Smith,(unknown),Pauline A. Filipek,Maureen Bocian,Charlotte Modahl,Pamela Flodman,M. Anne Spence	38
8	Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13 2000 ·American Journal of Medical Genetics ·Moyra Smith,Pauline A. Filipek,(unknown),Maureen Bocian,(unknown),Charlotte Modahl,M. Anne Spence	40
9	The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly 1999 ·Human Molecular Genetics ·Luisa Nanni,Jeffrey E. Ming,Maureen Bocian,Kathryn A. Steinhaus,Diana W. Bianchi,Christine de Die‐Smulders,Aldo Giannotti,K Imaizumi,Kenneth Lyons Jones,Miguel Del Campo,(unknown),(unknown),Mary Ella Pierpont,Nathaniel H. Robin,I.D. Young,Erich Roessler,Maximilian Muenke	274
10	Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma 1999 ·American Journal of Medical Genetics ·Chanin Limwongse,Stuart S. Schwartz,Maureen Bocian,Nathaniel H. Robin	30
11	A High-Resolution Physical and Transcript Map of the Cri du Chat Region of Human Chromosome 5p 1997 ·Genome Research ·Deanna M. Church,Julie L. Yang,Maureen Bocian,Rita Shiang,John J. Wasmuth	38
12	Multiple vertebral segmentation defects: Analysis of 26 new patients and review of the literature 1996 ·American Journal of Medical Genetics ·Geert Mortier,Ralph S. Lachman,Maureen Bocian,David L. Rimoin	82
13	Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization 1993 ·American Journal of Medical Genetics ·Renée Bernstein,Maureen Bocian,(unknown),Ulla Bengtsson,John J. Wasmuth	5
14	Hydrops fetalis in the McKusick-Kaufman syndrome: A case report 1991 ·American Journal of Obstetrics and Gynecology ·(unknown),Maureen Bocian	8
15	Importance of accurate diagnosis in counseling for neural tube defects diagnosed prenatally 1991 ·Clinical Genetics ·Kathryn A. Steinhaus,Renée Bernstein,Maureen Bocian	2
16	Interstitial deletion of the long arm of chromosome 3: Case report, review, and definition of a phenotype 1987 ·American Journal of Medical Genetics ·(unknown),Maureen Bocian,Ann P. Walker,John M. Opitz,James F. Reynolds	38
17	Familial diaphragmatic defects. Early prenatal diagnosis and evidence for major gene inheritance 1986 ·American Journal of Medical Genetics ·Maureen Bocian,M. Anne Spence,Mary L. Marazita,Ann P. Walker,(unknown),John M. Opitz,James F. Reynolds	9
18	Fetal Hydrocephalus and Ear Anomalies Associated with Maternal Use of Isotretinoin 1985 ·Obstetrical & Gynecological Survey ·Ira T. Lott,Maureen Bocian,Henry W. Pribram,(unknown)	1
19	Atypical biochemical findings in Turner’s syndrome: identification of a possible subset 1984 ·Fertility and Sterility ·Lubomir J. Valenta,Alan N. Elias,Maureen Bocian	6
20	Trisomy F(?20). Report of A 14q-F(?20) familial translocation. 1971 ·PubMed ·(unknown),(unknown),(unknown),Maureen Bocian	10

About Maureen Bocian

Maureen Bocian is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 35 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (8 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Genetics (1.4k citations), Developmental Biology (63 citations) and Molecular Biology (1.2k citations). Maureen Bocian has collaborated with scholars based in United States, United Kingdom and Japan. Frequent co-authors include John J. Wasmuth, Rita Shiang, Deanna M. Church, Thomas J. Fielder, Yazhen Zhu, Leslie M. Thompson, Sara T. Winokur, John M. Opitz, M. Anne Spence and Charlotte Modahl. Their work appears in journals such as Cell, Annals of Neurology and Genome Research.

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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