N. Freire‐Maia

2.9k total citations
138 papers, 1.9k citations indexed

About

N. Freire‐Maia is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, N. Freire‐Maia has authored 138 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 38 papers in Molecular Biology and 12 papers in Genetics. Recurrent topics in N. Freire‐Maia's work include dental development and anomalies (21 papers), Hemoglobinopathies and Related Disorders (11 papers) and Skin and Cellular Biology Research (9 papers). N. Freire‐Maia is often cited by papers focused on dental development and anomalies (21 papers), Hemoglobinopathies and Related Disorders (11 papers) and Skin and Cellular Biology Research (9 papers). N. Freire‐Maia collaborates with scholars based in Brazil, United States and Chile. N. Freire‐Maia's co-authors include Marta Pinheiro, Ademar Freire‐Maia, Francisco M. Salzano, John M. Opitz, H. Krieger, Eleidi A. Chautard‐Freire‐Maia, James F. Reynolds, Iglenir João Cavalli, I. Cat and B. Arce-Gomez and has published in prestigious journals such as Nature, Science and The Lancet.

In The Last Decade

N. Freire‐Maia

132 papers receiving 1.7k citations

Peers

N. Freire‐Maia

MB

GENET

OS

GENET

CB

Matthew Edwards Australia

Cheng‐Ming Chuong United States

Ahmad S. Teebi Canada

C. S. Chung United States

Margaret E. Cooper United States

J. Abbott United States

Yasuo Nakagome Japan

John Rogers Australia

A Garner United Kingdom

Bradford Cannon United States

Matthew Edwards Australia

N. Freire‐Maia

1.1k ×1.3

MB

621 ×1.0

GENET

74 ×0.3

OS

113 ×0.6

GENET

179 ×1.1

CB

Citations per year, relative to N. Freire‐Maia N. Freire‐Maia (= 1×) peers Matthew Edwards

Countries citing papers authored by N. Freire‐Maia

Since Specialization

Citations

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

Fields of papers citing papers by N. Freire‐Maia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. Freire‐Maia. 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 N. Freire‐Maia. The network helps show where N. Freire‐Maia may publish in the future.

Co-authorship network of co-authors of N. Freire‐Maia

This figure shows the co-authorship network connecting the top 25 collaborators of N. Freire‐Maia. A scholar is included among the top collaborators of N. Freire‐Maia 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 N. Freire‐Maia. N. Freire‐Maia 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

1.

Pinheiro, Marta & N. Freire‐Maia. (1985). Atrichias and Hypotrichoses: A Brief Review with Description of a Recessive Atrichia in two Brothers. Human Heredity. 35(1). 53–55. 12 indexed citations

2.

Cavalli, Iglenir João, I.J. Sbalqueiro, Anita Wajntal, & N. Freire‐Maia. (1982). A 15/17 Translocation in a Patient with Prader-Labhart-Willi Syndrome. Human Heredity. 32(3). 149–151. 12 indexed citations

3.

Freire‐Maia, N., et al.. (1981). Anthropometric Data of Children Heterozygous for Abnormal Hemoglobins (Hb AS, Hb AC) and Paired Controls Hb AA. Human Heredity. 31(2). 70–73. 1 indexed citations

4.

Freire‐Maia, N., et al.. (1978). Genetic Investigations in a Northern Brazilian Island. Human Heredity. 28(5). 386–396. 8 indexed citations

5.

Freire‐Maia, N., et al.. (1978). Genetic Investigations in a Northern Brazilian Island. Human Heredity. 28(6). 401–410. 12 indexed citations

6.

Cohen, Marc, et al.. (1977). AMG volume 26 issue 2 Cover and Front matter. Acta geneticae medicae et gemellologiae. 26(2). f1–f1. 1 indexed citations

7.

Freire‐Maia, N., et al.. (1977). An Ectodermal Dysplasia Syndrome of Alopecia, Onychodysplasia, Hypohidrosis, Hyperkeratosis, Deafness and other Manifestations. Human Heredity. 27(2). 127–133. 10 indexed citations

8.

Freire‐Maia, N.. (1976). Genetic Loads in Man. Human Heredity. 26(2). 95–104. 6 indexed citations

9.

Freire‐Maia, Ademar, N. Freire‐Maia, & William J. Schull. (1975). Genetics of Acheiropodia (‘the Handless and Footless Families of Brazil’). Human Heredity. 25(4). 329–336. 6 indexed citations

10.

Freire‐Maia, N.. (1975). A Heterozygote Expression of a ‘Recessive’ Gene?. Human Heredity. 25(4). 302–304. 6 indexed citations

11.

Karam, Elie G., et al.. (1974). Consanguineous Marriages and Umbilical Tetanus in Brazilian Populations. Human Heredity. 24(1). 75–81. 1 indexed citations

12.

Cat, I., et al.. (1972). Odontotrichomelic Hypohidrotic Dysplasia A Clinical Reappraisal. Human Heredity. 22(1). 91–95. 7 indexed citations

13.

Arce-Gomez, B., et al.. (1970). A Genetic Study on Palatolabial Defects. Human Heredity. 20(6). 580–589. 3 indexed citations

14.

Freire‐Maia, N., et al.. (1970). Inbreeding Load, as Estimated with Sib Control, in a Portuguese Population. Human Heredity. 20(3). 248–251. 5 indexed citations

15.

Freire‐Maia, N., et al.. (1968). P.T.C. Sensitivity Among Psychiatric Patients. Human Heredity. 18(1). 31–37. 11 indexed citations

16.

Freire‐Maia, N. & Ademar Freire‐Maia. (1967). Recurrence Risks of Bone Aplasias and Hypoplasias of the Extremities. Human Heredity. 17(5). 418–421. 3 indexed citations

17.

Freire‐Maia, N.. (1963). The Load of Lethal Mutations in White and Negro Brazilian Populations II. Second Survey. Human Heredity. 13(3). 199–225. 19 indexed citations

18.

Freire‐Maia, N., et al.. (1963). The Load of Lethal Mutations in White and Negro Brazilian Populations I. First Survey. Human Heredity. 13(3). 185–198. 25 indexed citations

19.

Salzano, Francisco M., et al.. (1962). Genetic Load in Brazilian Indians. Human Heredity. 12(3-4). 212–218. 7 indexed citations

20.

Freire‐Maia, N.. (1952). Frequencies of consanguineous marriages in Brazilian populations.. PubMed. 4(3). 194–203. 24 indexed citations

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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