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D-Index & Metrics

Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Genetics 75 1888 1796 237 228 224 25272

Fiona Lalloo publications per year

The chart shows the history of publications by Fiona Lalloo between 1991 and 2025, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Fiona Lalloo published across 35 years, from 1991 to 2025, averaging 7.9 papers a year. Output peaked at 34 publications in 2021. 11 of the 275 publications appeared in the last two years.

No. of publications
10 20 30
Bar chart. Horizontal axis: year, 1991 to 2025. Vertical axis: number of publications, 0 to 34. Peak 34 publications in 2021. 1991: 1 publication 1992: 0 publications 1993: 0 publications 1994: 0 publications 1995: 0 publications 1996: 0 publications 1997: 1 publication 1998: 3 publications 1999: 8 publications 2000: 4 publications 2001: 5 publications 2002: 7 publications 2003: 8 publications 2004: 9 publications 2005: 7 publications 2006: 7 publications 2007: 5 publications 2008: 8 publications 2009: 12 publications 2010: 16 publications 2011: 11 publications 2012: 11 publications 2013: 14 publications 2014: 7 publications 2015: 8 publications 2016: 7 publications 2017: 14 publications 2018: 13 publications 2019: 6 publications 2020: 18 publications 2021: 34 publications 2022: 8 publications 2023: 12 publications 2024: 9 publications 2025: 2 publications
1991 2025

275 publications in total across all disciplines

View publications per year as a table
Fiona Lalloo: publications per year, 1991 to 2025
Year Publications
1991 1
1992 0
1993 0
1994 0
1995 0
1996 0
1997 1
1998 3
1999 8
2000 4
2001 5
2002 7
2003 8
2004 9
2005 7
2006 7
2007 5
2008 8
2009 12
2010 16
2011 11
2012 11
2013 14
2014 7
2015 8
2016 7
2017 14
2018 13
2019 6
2020 18
2021 34
2022 8
2023 12
2024 9
2025 2
Total 275
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Fiona Lalloo publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Fiona Lalloo sits on this spectrum.

No. of scientists
50 100 150 200
Bar chart with 67 bars. Horizontal axis: publications, 45–54 to 703+. Vertical axis: number of scientists, 0 to 217. Most scientists, 217, have 125–134 publications. The last bar groups every scientist with 703 publications or more. The highlighted bar, 215–224 publications, is where this scientist sits. 45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45–54 publications 703+

This scientist: 224 publications — 59th percentile

59% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

View publications distribution as a table
Number of Genetics scientists by publication count, Research.com 2026 ranking edition. Based on 4,342 ranked scientists.
Publications Scientists This scientist
45–54 6
55–64 10
65–74 35
75–84 84
85–94 102
95–104 151
105–114 175
115–124 203
125–134 217
135–144 205
145–154 193
155–164 188
165–174 170
175–184 178
185–194 164
195–204 173
205–214 159
215–224 134 224
225–234 143
235–244 105
245–254 114
255–264 92
265–274 88
275–284 87
285–294 80
295–304 62
305–314 75
315–324 67
325–334 60
335–344 52
345–354 40
355–364 48
365–374 47
375–384 46
385–394 31
395–404 27
405–414 40
415–424 30
425–434 43
435–444 29
445–454 14
455–464 28
465–474 21
475–484 21
485–494 22
495–504 17
505–514 12
515–524 11
525–534 8
535–544 8
545–554 14
555–564 4
565–574 11
575–584 5
585–594 11
595–604 12
605–614 7
615–624 6
625–634 10
635–644 9
645–654 10
655–664 6
665–674 6
675–684 6
685–694 4
695–702 6
703+ 100
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Fiona Lalloo D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Fiona Lalloo sits on this spectrum.

No. of scientists
50 100 150
Bar chart with 61 bars. Horizontal axis: D-Index, 40–41 to 160+. Vertical axis: number of scientists, 0 to 191. Most scientists, 191, have 62–63 D-Index. The last bar groups every scientist with 160 D-Index or more. The highlighted bar, 74–75 D-Index, is where this scientist sits. 40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40–41 D-Index 160+

This scientist: 75 D-Index — 57th percentile

57% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

View D-Index distribution as a table
Number of Genetics scientists by D-index, Research.com 2026 ranking edition. Based on 4,342 ranked scientists.
D-Index Scientists This scientist
40–41 24
42–43 52
44–45 84
46–47 112
48–49 118
50–51 141
52–53 143
54–55 145
56–57 179
58–59 162
60–61 175
62–63 191
64–65 172
66–67 184
68–69 164
70–71 158
72–73 150
74–75 136 75
76–77 127
78–79 127
80–81 111
82–83 110
84–85 110
86–87 84
88–89 102
90–91 66
92–93 72
94–95 70
96–97 54
98–99 60
100–101 49
102–103 55
104–105 45
106–107 42
108–109 28
110–111 39
112–113 25
114–115 31
116–117 29
118–119 34
120–121 29
122–123 29
124–125 18
126–127 27
128–129 22
130–131 16
132–133 11
134–135 17
136–137 12
138–139 21
140–141 4
142–143 9
144–145 14
146–147 6
148–149 10
150–151 7
152–153 9
154–155 8
156–157 8
158–159 9
160+ 96
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Overview

Fiona Lalloo is affiliated with the University of Manchester in the United Kingdom. Their research focuses primarily on genetics and oncology, with a broad scope encompassing molecular biology and cancer research.

Their recent publications cover a range of topics related to genetic predispositions, cancer genetics, and molecular mechanisms. Notable papers include:

  • Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriers (2020, Genetics in Medicine)
  • Eflornithine plus Sulindac for Prevention of Progression in Familial Adenomatous Polyposis (2020, New England Journal of Medicine)
  • Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells (2022, Nature Communications)
  • Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group (2021, Familial Cancer)
  • The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant (2021, Genetics in Medicine)

The core topics of Fiona Lalloo's work include:

  • BRCA gene mutations in cancer
  • Genetic factors in colorectal cancer
  • Cancer Genomics and Diagnostics
  • DNA Repair Mechanisms
  • Global Cancer Incidence and Screening
  • Ovarian cancer diagnosis and treatment
  • Genomic variations and chromosomal abnormalities

Lalloo's research is published frequently in the following venues:

  • Journal of Medical Genetics
  • Genetics in Medicine
  • Cancers
  • Familial Cancer
  • European Journal of Human Genetics

Collaboration is a significant aspect of their work, with frequent co-authors including:

  • D. Gareth Evans
  • Emma R. Woodward
  • Anthony Howell
  • Sacha J. Howell
  • Elaine F. Harkness

Fiona Lalloo's main fields of study reflect an interdisciplinary approach involving:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Subfields of particular focus within their research include:

  • Genetics
  • Oncology
  • Cancer Research
  • Pathology and Forensic Medicine
  • Molecular Biology

Best Publications

  • Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies

    A. Antoniou;P.D.P. Pharoah;S. Narod;H.A. Risch

  • Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register service.

    D.G. Evans;E. Howard;E. Howard;C. Giblin;C. Giblin;T. Clancy;T. Clancy

  • Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype

    Sunil R. Lakhani;Jorge S. Reis-Filho;Laura Fulford;Frederique Penault-Llorca

  • The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.

    A C Antoniou;A P Cunningham;J Peto;D G Evans

  • Germline mutations in RAD51D confer susceptibility to ovarian cancer

    Chey Loveday;Clare Turnbull;Emma Ramsay;Deborah Hughes

  • Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

    Pål Møller;Toni T Seppälä;Inge Bernstein;Inge Bernstein;Elke Holinski-Feder

  • Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

    Pal Moller;Toni Seppala;Inge Bernstein;Inge Bernstein;Elke Holinski-Feder

  • Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

    Bryony A Thompson;Bryony A Thompson;Amanda B Spurdle;John-Paul Plazzer;Marc S Greenblatt

  • Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations in SDHB and SDHD

    Christopher J. Ricketts;Julia R. Forman;Eleanor Rattenberry;Nicola Bradshaw

  • Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG)

    Kevin J Monahan;Nicola Bradshaw;Sunil Dolwani;Bianca Desouza

  • Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

    Roger L Milne;Roger L Milne;Karoline B Kuchenbaecker;Karoline B Kuchenbaecker;Kyriaki Michailidou;Kyriaki Michailidou;Jonathan Beesley

  • Cumulative lifetime incidence of extracolonic cancers in Lynch syndrome: a report of 121 families with proven mutations

    Emma Barrow;L. Robinson;W. Alduaij;A. Shenton

  • Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programme

    E Amir;D G Evans;A Shenton;F Lalloo

  • Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations.

    Anthony Moran;C O'Hara;S Khan;Lorraine G Shack

  • Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

    Susan L. Neuhausen;Sylvie Mazoyer;Lori Friedman;Michael Stratton

  • Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers

    Karoline B Kuchenbaecker;Karoline B Kuchenbaecker;Lesley McGuffog;Daniel Barrowdale;Andrew Lee

  • A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.

    D G R Evans;D M Eccles;N Rahman;K Young

  • Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: Risks of breast/ovarian cancer quoted should reflect the cancer burden in the family

    D Gareth R Evans;Andrew Shenton;Emma Woodward;Fiona Lalloo

Frequent Co-Authors

D. Gareth Evans
D. Gareth Evans University of Manchester
Anthony Howell
Anthony Howell University of Manchester
Antonis C. Antoniou
Antonis C. Antoniou University of Cambridge
Diana Eccles
Diana Eccles University of Southampton
Douglas F. Easton
Douglas F. Easton University of Cambridge
Heli Nevanlinna
Heli Nevanlinna University of Helsinki
Paolo Radice
Paolo Radice Fondazione IRCCS Istituto Nazionale dei Tumori
Katherine L. Nathanson
Katherine L. Nathanson University of Pennsylvania
Georgia Chenevix-Trench
Georgia Chenevix-Trench QIMR Berghofer Medical Research Institute

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