Blanche P. Alter

19.8k total citations
273 papers, 11.3k citations indexed

About

Blanche P. Alter is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Blanche P. Alter has authored 273 papers receiving a total of 11.3k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Molecular Biology, 89 papers in Physiology and 78 papers in Genetics. Recurrent topics in Blanche P. Alter's work include DNA Repair Mechanisms (53 papers), Blood disorders and treatments (52 papers) and Hemoglobinopathies and Related Disorders (51 papers). Blanche P. Alter is often cited by papers focused on DNA Repair Mechanisms (53 papers), Blood disorders and treatments (52 papers) and Hemoglobinopathies and Related Disorders (51 papers). Blanche P. Alter collaborates with scholars based in United States, Canada and United Kingdom. Blanche P. Alter's co-authors include Philip S. Rosenberg, Sharon A. Savage, Neelam Giri, Akiko Shimamura, David G. Nathan, Mark H. Greene, Gabriela M. Baerlocher, Neal S. Young, Peter M. Lansdorp and Sabra C. Goff and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Blanche P. Alter

266 papers receiving 10.8k citations

Peers

Countries citing papers authored by Blanche P. Alter

Since Specialization

Citations

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

Fields of papers citing papers by Blanche P. Alter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Blanche P. Alter. 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 Blanche P. Alter. The network helps show where Blanche P. Alter may publish in the future.

Co-authorship network of co-authors of Blanche P. Alter

This figure shows the co-authorship network connecting the top 25 collaborators of Blanche P. Alter. A scholar is included among the top collaborators of Blanche P. Alter 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 Blanche P. Alter. Blanche P. Alter 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	Reduced anti-Müllerian hormone levels in males with inherited bone marrow failure syndromes 2024 ·Endocrine Connections ·Pamela Stratton, Neelam Giri, (unknown), (unknown), Blanche P. Alter, Sharon A. Savage, Lígia A. Pinto	0
2	Germline mutation of MDM4 , a major p53 regulator, in a familial syndrome of defective telomere maintenance 2020 ·Science Advances ·Eléonore Toufektchan, (unknown), (unknown), Neelam Giri, Irena Drašković, Boris Bardot, (unknown), Sara Jaber, Blanche P. Alter, Arturo Londoño‐Vallejo, Sharon A. Savage, Franck Toledo	27
3	Phenotypes of Diamond Blackfan Anemia Patients with RPL35A Haploinsufficiency Due to 3q29 Deletion Compared with RPL35A Single Nucleotide Variants or Small Insertion/Deletions 2018 ·Blood ·Neelam Giri, Matthew Gianferante, (unknown), Marcin W. Włodarski, Paola Quarello, (unknown), (unknown), Vijay G. Sankaran, Jason E. Farrar, Maryam Hussain, Lisa J. McReynolds, Antonis Kattamis, Jeffrey M. Lipton, Charlotte M. Niemeyer, Dagmar Pospı́šilová, Ugo Ramenghi, Sharon A. Savage, Adrianna Vlachos, Blanche P. Alter	2
4	Inherited bone marrow failure syndromes: considerations pre- and posttransplant 2017 ·Hematology ·Blanche P. Alter	27
5	Prognostic Significance of Pulmonary Function Test Abnormalities in Patients with Dyskeratosis Congenita 2016 ·Blood ·Neelam Giri, (unknown), Joseph A. Fontana, Blanche P. Alter, Payal P. Khincha, Sharon A. Savage	0
6	Research participant interest in primary, secondary, and incidental genomic findings 2016 ·Genetics in Medicine ·Jennifer T. Loud, Renée C. Bremer, L. Phuong, June A. Peters, Neelam Giri, Douglas R. Stewart, Mark H. Greene, Blanche P. Alter, Sharon A. Savage	20
7	Novel FANCI mutations in Fanconi anemia with VACTERL association 2015 ·American Journal of Medical Genetics Part A ·Sharon A. Savage, Bari J. Ballew, Neelam Giri, Settara C. Chandrasekharappa, Najim Ameziane, Johan de Winter, Blanche P. Alter, (unknown)	19
8	Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families 2014 ·Blood ·(unknown), Elizabeth R. Macari, Lea Jessop, Steven R. Ellis, Timothy A. Myers, Neelam Giri, Alison M. Taylor, (unknown), (unknown), Bari J. Ballew, Meredith Yeager, Joseph F. Boland, Ji He, Belynda Hicks, Laurie Burdett, Blanche P. Alter, Leonard I. Zon, Sharon A. Savage	69
9	Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1 2014 ·Genes & Development ·(unknown), Bari J. Ballew, Kamlesh Bisht, (unknown), Belynda Hicks, Shalabh Suman, (unknown), Neelam Giri, (unknown), Ivan Maillard, Blanche P. Alter, Catherine E. Keegan, Jayakrishnan Nandakumar, Sharon A. Savage	86
10	The use of haematopoietic stem cell transplantation in Fanconi anaemia patients: a survey of decision making among families in the US and Canada 2013 ·Health Expectations ·Sadie P. Hutson, Paul K. J. Han, Jada G. Hamilton, Sean C. Rife, (unknown), Richard P. Moser, (unknown), (unknown), Blanche P. Alter	8
11	The relationship between DNA methylation and telomere length in dyskeratosis congenita 2011 ·Aging Cell ·Shahinaz M. Gadalla, Hormuzd A. Katki, Fatma M. Shebl, Neelam Giri, Blanche P. Alter, Sharon A. Savage	24
12	Pathophysiology and management of inherited bone marrow failure syndromes 2010 ·Blood Reviews ·Akiko Shimamura, Blanche P. Alter	327
13	TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita 2008 ·The American Journal of Human Genetics ·Sharon A. Savage, Neelam Giri, Gabriela M. Baerlocher, Nick Orr, Peter M. Lansdorp, Blanche P. Alter	285
14	Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita 2007 ·Blood ·Blanche P. Alter, Gabriela M. Baerlocher, Sharon A. Savage, Stephen J. Chanock, Babette B. Weksler, Judith P. Willner, June A. Peters, Neelam Giri, Peter M. Lansdorp	248
15	Thrombocytopenia, multiple mucosal squamous cell carcinomas, and dyspigmentation 2006 ·Journal of the American Academy of Dermatology ·(unknown), Neelam Giri, Blanche P. Alter, Edward W. Cowen	2
16	Risk of head and neck squamous cell cancer and death in patients with Fanconi anemia who did and did not receive transplants 2004 ·Blood ·Philip S. Rosenberg, Gèrard Socié, Blanche P. Alter, Éliane Gluckman	191
17	Die laparoskopische Hernioplastik nach dem TAPP-Verfahren: Eine Analyse und Nachbeobachtung von 267 Fällen 2004 ·Zentralblatt für Chirurgie - Zeitschrift für Allgemeine Viszeral- Thorax- und Gefäßchirurgie ·Blanche P. Alter, (unknown), (unknown), (unknown)	5
18	Pure Red Cell Aplasia Associated With Hepatitis C Infection 1997 ·The American Journal of the Medical Sciences ·(unknown), David Sears, George Carrum, Mark M. Udden, Blanche P. Alter, (unknown)	6
19	Childhood red cell aplasia 1980 ·Journal of Pediatric Hematology/Oncology ·Blanche P. Alter	45
20	Pupillotonia, hyporeflexia, and segmental hypohidrosis: Autonomic dysfunction in a child 1968 ·The Journal of Pediatrics ·Nancy B. Esterly, (unknown), Blanche P. Alter, Saul W. Brusilow	20

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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